Statins are currently being eyed for use in management of a variety of ocular pathologies of vitreoretinal origin, including AMD [2, 22, 47]. However results with clinical studies were only moderately promising [2, 22, 24, 48] and were based on the clinical evidence and/or the pharmacodynamic effects [21, 49]; and none of the studies confirmed whether significant drug reached the ocular tissues so as to elicit a measurable physiological response. It is important that following oral administration, sufficient statin crosses the blood-aqueous barrier and reaches the internal eye to produce an effect. Statins are poorly bioavailable (5–14%; ATS 12%), and it may be noted that only a small proportion (generally 1/3 to 1/5) of the concentration of any drug in plasma, reaches the aqueous/vitreous humor [50, 51]. Although retinal availability of lipophilic drugs like statins following systemic administration can also occur via the choroid tissue, the high molecular weight (> 500 Da) is a limitation for this pathway [52].
We presently developed an eye drop formulation of ATS for achieving high local concentration in the ocular tissue. Challenges to achieving this were manifold: (i) insolubility (0.00495 mg/ml) of ATS, (ii) circumventing ocular barriers to reach the posterior eye including multiple drainage pathways, and (iii) high molecular weight of ATS (557.63 Da) which limits its permeation.
Significant work is published on solubility and bioavailability enhancement of ATS following oral administration. Solid dispersion of ATS using various polymers, viz. PEG 4000, PVK 30, and Kollicoat IR, has been prepared and reported [53, 54]. In addition to poor solubility, extensive first-pass metabolism limits the oral bioavailability of ATS to < 15% and it is argued that solid dispersions can only improve the former, but once absorbed, ATS will still undergo first-pass effect. Hence, it was proposed that encapsulation within a slow release nanoparticulate system can manage both solubility and metabolism issues. Polymeric nanoparticles of ATS with sufficient encapsulation (nearly 70%) and extended release were thus prepared by some groups [55,56,57,58]. Sripriyalakshmi et al. prepared ATS-loaded albumin nanoparticles by desolvation method, using glutaraldehyde (8%) as cross-linker and ethanol as a precipitating agent [59]. Kumar et al. developed ATS-SLNs through hot homogenization technique using trimyristin and soy-phosphatidylcholine as lipids. For preparing lipid drug matrix, a mixture of chloroform–methanol was used [60]. Similarly ATS-SLNs by solvent injection technique are also reported [61]. However, use of cross-linking agents and organic solvents and a residual contamination with these can be a concern in ocular delivery. Polymerization initiation, formation of toxic monomers and degradation products, and large polymer aggregates are also a limitation with polymeric systems [62, 63]. Other problems include lack of large-scale production method [64] and a suitable sterilization method, e.g., autoclaving.
To address all these limitations, an optimized ATS-loaded solid lipid nanoparticulate system was developed presently which is an aqueous system comprising ingredients employed at concentrations approved to be safe by USFDA [65] for ocular use. Further, the methodology used, i.e., high-pressure homogenization, is scalable and industrially viable.
Prescreening studies
SLNs comprise a nanosized lipidic core stabilized by a layer of surfactants. Selection of lipid and surfactant and their concentration are thus an important consideration for development of SLNs. However, high proneness of ATS to degradation, including oxidation in surfactant solutions especially polysorbate 80 (the most commonly employed surfactant in pharmaceutical formulations), was a serious challenge to its solubilization for preparing SLNs [32]. A series of surfactants and solvents, viz. Transcutol P, propylene glycol, Poloxamer (P) 188, PEG 300, PEG 400, and PEG 600, were thus tried in the initial prescreening studies for formation of ATS-SLNs. Minimum volume of surfactant required to completely dissolve the required quantity of ATS (0.25% w/v) along with protection from oxidation and hydrolysis was taken as criteria for their selection. However, safety and biocompatibility of selected components at their employed concentrations with ocular tissues and their amenability to steam sterilization were also a consideration [66].
Highest solubility of ATS was noticed in PEG 400 (56 mg/ml); hence, it was selected as a solubilizer. To improve drug loading and entrapment efficiency, it is important that the drug is incorporated in the SLN matrix in a soluble form [67] and for that purpose, an optimized concentration of PEG 400 was employed. Among the surfactants, not only did a 4% solution of P 188 enhance the solubility of ATS by 100 times (0.04 mg/ml), but also ATS was found to be stable (7 days) in this solution; hence, it was selected as the surfactant of choice. Both P 188 and PEG 400 can help achieve small size, high loading, and significant entrapment. Both these agents are permeation enhancers [68, 69], and PEG also has a P-gp efflux–inhibiting property. In addition, PEG is a surfactant-supporting polymer which is known to reduce the gelation of SLNs [61]. P 188 protects against oxidation by getting adsorbed on the surface of lipidic nanoparticles due to its large hydrophilic blocks providing barrier for free radical chain reaction [70].
Even though ATS is a lipophilic molecule (log P = 4.41), yet it was not soluble in any of the lipids, viz. Compritol® 888 ATO, glyceryl monostearate, stearic acid, and Precirol® ATO 5, screened by us. Considering our prior experience with Compritol® 888 ATO for developing SLNs for a variety of drug molecules, its ability to form stable SLNs of sufficiently small size and its biocompatibility with ocular tissue [71], it was selected presently as the lipid matrix. Soya lecithin (Phospholipon 90H) was used as a co-surfactant and its addition improved the entrapment efficiency and stability of ATS-SLNs [72]. It is reported that oxidative stress is the initial pathological mechanism in the development of AMD which leads to oxidation of phospholipids present in the photoreceptors [73]. Excess accumulation of oxidized phosphatidylcholine was observed in immunohistochemistry of the eyes with AMD [13]. Hence, it is proposed that the anti-oxidant nature [74] of P 90H (i) will help in reducing the oxidative stress of AMD eyes and (ii) may also restore the level of unoxidized phospholipid in the photoreceptors.
Screening studies and optimization of ATS-SLNs
Based on the above-discussed facts and the results of Table 1 and Supplementary data, and on our prior experience in the lab, a range of concentration of various components, viz. Compritol® 888 ATO, P90H, P 188, and PEG 400, was selected. SLN dispersions, which were stable for more than a week, were characterized for TDC, EE, and particle size. On the basis of stability of dispersion, the minimum and maximum of each component were selected. The selected CMAs were varied in the range of 1–5% w/w for Compritol® 888 ATO, 1–2% w/w for P 90H, 1.5–5% w/w for P 188, and 2–4% for PEG 400, in the optimization studies. Drug concentration varied from 0.2 to 0.5% w/w, and it was observed that an increase beyond 0.25% w/w tended to decrease the EE; hence, ATS concentration was fixed at 0.25% for further optimization. Based on preliminary experiments, various process variables were also fixed at particular levels like—the number of HPH cycles was fixed at 3, because 4 or higher number of passage through HPH resulted in an increase in size by 20–30 nm per cycle; likewise, stirring speed and time of stirring for preparation of the coarse preemulsion was fixed at 9000 rpm for 8 min. Further increase in stirring speed and time resulted in a decrease in entrapment efficiency, and below the selected levels, bigger particles were observed.
Systematic optimization of ATS-SLNs
FDA recommends that the design of pharmaceutical products [75] should involve a “quality-by-design” approach; hence, an optimized ATS-SLN formulation was designed presently employing CCD as per standard protocol (Table 1) using a desirability approach.
Regression analysis of experimental design
In the analysis of optimization experiment, a second-order function (response surface) was used to characterize the effect of independent variables (X1—Compritol® 888 ATO/P90H; X2—P 188/PEG 400) on the particle size and entrapment efficiency (responses). Produced data for the responses were regressed to obtain the coefficients including interaction term [76]. Regression analysis was facilitated by coding of the factor in order to simplify the analysis. The generated polynomial mathematical equation for the responses is represented and tabulated in Table 2 along with the significance (p value).
Table 2 Summary of various factor effects and their p values for responses Y1 and Y2
Polynomial mathematical equations defined by CCD are as follows:
$$ {Y}_1=276.79+124.75{X}_1-23.97{X}_2-3.55{X}_1{X}_2+141.27{X_1}^2+48.12{X_2}^2. $$
$$ {Y}_2=82.08+2.12{X}_1+2.50{X}_2+7.13{X}_1{X}_2-11.72{X_1}^2-2.67{X_2}^2. $$
The sign and magnitude of the effects in each equation signify the relative influence of each factor on the response. A negative sign signifies an antagonistic effect while a positive sign indicates a synergistic effect. Negative correlation of particle size was observed with the increase in the ratio of P 188/PEG 400. Combined effect (interaction term) of both CMAs also exhibited a negative influence on particle size. Further, p value (< 0.05) of individual factors demonstrated that the ratio of Compritol® 888 ATO/P 90H as such, as well as in its square term, has a significant contribution to the variability in particle size. For EE, the most significant factors were quadratic term of Compritol® 888 ATO/P 90H ratio and interaction of both CMAs which had p values < 0.005. Both CMAs as such and their combined effect showed positive correlation with EE, but their quadratic terms found a negative influence on EE (Table 2).
Table 3 represents the result of ANOVA test on the quadratic regression model and details the model summary statistics for the selected significant quadratic models. The quadratic model was statistically significant (p < 0.001) in both cases while the lack of fit was insignificant (p > 0.05). It can be observed from Table 3 that all responses had r2 value > 0.9, which indicates a good correlation between the experimental and the predicted responses. Further, the selected models explain a significant proportion of variability in the observed responses (F ratio test, p value < 0.001). Adequate precision measures the signal-to-noise ratio and a value > 4 indicates good reliability [33].
Table 3 Model summary statistics of the quadratic response surface model
For further establishing the appropriateness of the selected models, several diagnostic plots like normal plot of residuals and Box–Cox plot (not shown), were used to establish its appropriateness and goodness of fit of the data. The plots also confirmed that CCD matrix data was free from outlier variables and did not require any transformation.
The relationship between formulation variables for preparing ATS-SLNs and the resulting response is summarized graphically (Fig. 1) by the response surface plots obtained from the modeling steps. The particle size was found to decrease with the increase in Compritol® 888 ATO/P 90H ratio from 0.5 to 2.5. Beyond 2.5, SLNs of higher particle size were observed as shown in Fig. 1a. This increase in particle size beyond a certain lipid concentration is probably due to an increase in viscosity of developed system resulting in agglomeration of particles [77]. Increase in the P 188/PEG400 ratio resulted in a decrease in particle size up to mid-level and after that, particle size increased. Similar concentration-dependent surfactant and co-surfactant effect of P 188 on particle size of paclitaxel-loaded polymeric nanoparticles has been reported [58]. It seems that the hydrophobic propylene chain of P 188 aligns on the lipid/water interface along with PEG and P90H to cover the melted lipid droplets more efficiently, thus reducing the interfacial tension at the lipid–water interface, resulting in a lower particle size. Further, P 188 may also offer steric stabilization to formed particles, thus avoiding their aggregation. However, as the concentration of P 188 increases beyond a certain level (3.25% in this case), the hydrophilic (PEG) chains of one particle of P 188 may interact with those of the other particles. These inter-particle interactions can result in agglomeration at higher concentrations [78].
Entrapment efficiency of SLNs initially increased with an increase in the Compritol® 888 ATO/P 90H ratio, while a further increase (> 2.5) resulted in a decrease in percentage EE as shown in Fig. 1b. The initial increment in EE can be attributed to availability of a sufficient Compritol® 888 ATO to completely encapsulate ATS (fixed at 0.25% w/v) complemented with an adequate quantity of P 90H. Compritol® 888 ATO is a complex lipid composed of mixtures of mono-, di-, and triglycerides which form less perfect crystals, and thus accord space to accommodate drug molecules [79]. P 90H is also reported to create space for drug incorporation, and the monomolecular P 90H layer stabilizes the particle interface [80]. A decrease in percentage EE at a high ratio of Compritol® 888 ATO/P 90H can be attributed to the availability of a lesser quantity of P 90H with respect to Compritol® 888 ATO.
Increase in percentage EE was also noticed with an increase in the ratio of P 188/PEG 400. However, at an extreme ratio, i.e., from 2.0 to 2.5, a significant decrease in the percentage EE of the prepared SLNs was observed. PEG 400 has a high affinity for water and since ATS had a very high solubility (56 mg/ml versus 0.00495 mg/ml in water) in PEG 400, hence at a high P 188/PEG400 ratio, the proportion of PEG 400 being small will partition towards water-carrying ATS with it resulting in its low entrapment in the lipid matrix [81].
Selection of optimum formulation and validation
Minimum particle size and maximum EE were set as the selection criteria for finding optimum formulation. Based on these criteria, the software generated a single, most suitable solution, comprising the Compritol® 888 ATO/P 90H ratio 2.5 and P 188/PEG400 ratio 1.73 (Table 4). To check the reliability of the developed mathematical models, the response of the optimal SLN formulation and three additional checkpoint formulations covering the entire range of the experimental domain was recorded. For each of these test runs, the experimentally determined response was compared with the response predicted by the mathematical model. Table 4 lists the test conditions of the optimum and the random check points and their experimental and predicted values for both the response variables, along with the calculated percentage prediction error. Supplementary Fig. 1 (a, b) shows linear (r2 > 0.9) correlation plots between the observed and predicted response variables, indicating excellent goodness of fit. Low percentage prediction error (− 6.5 to 4.5 for Y1 and − 4.35 to 1.11 for Y2) and significant r2 confirm robustness of the mathematical model and high prognostic ability of response surface methodology.
Table 4 The experimental and predicted values for responses Y1 and Y2 along with percentage prediction error observed for the optimum test condition and random checkpoints Characterization of SLNs
Morphology of ATS-SLNs using optical and transmission electron microscopy
Optical inspection indicated the ATS-SLNs to be small in size and round in shape, with no aggregation or irregularities (Fig. 2). Similar results were obtained with TEM. The ATS-SLNs were found to be spherical in shape (Fig. 3), and the size of observed particles invariably varied between 70 and 185 nm. The TEM photograph at a higher magnification indicates differently transmitting areas in a single SLN particle (Fig. 3b). These may be due to P 90H, ATS, and PEG interspersed in the lipid matrix with uniform distribution (no core or shell structure is observed) as also indicated by a sustained release (Fig. 4) of ATS with no burst release. A surfactant layer enclosing the solid–lipid matrix is also observable in Fig. 3b. The former explains the larger hydrodynamic diameter [82] observed as measured by differential light scattering (DLS) (“Particle size and zeta potential”).
Particle size and zeta potential
The developed ATS-SLNs showed an average particle size (n = 6) of 256.3 ± 10.5 nm and PDI of 0.26 ± 0.02 (n = 6) (Supplementary Fig. 2). The PDI < 0.3 indicates a narrow particle size distribution. Small size offers a greater surface area for association and permeation through the cornea and conjunctiva [83]. Ample evidence of achieving therapeutic concentration of actives in the posterior eye tissue (including the retina) using these systems is indicated [84]. However, size is shown to influence the extent of absorption/permeation and disposition through the ocular static and dynamic barriers. Sakurai et al. studied the intraocular permeation efficiency of fluorescein-labeled polystyrene nanospheres of varying size (50, 200, 2000 nm). They observed that nanospheres with the particle size 200 nm could penetrate up to the retina while the particle size 2000 nm could not reach the retina and was seen in the vitreous cavity and trabecular meshwork only [85]. Similarly, uptake of PLGA particles in rabbit conjunctival epithelial cells was found to be higher for 100-nm particles in comparison with the corresponding 800-nm and 10,000-nm particles [86]. Size-dependent in vivo corneal uptake of indomethacin-loaded poly(epsilon-caprolactone) colloidal particles also indicates higher permeation of nanosized particles than microparticles after topical instillation into the albino rabbit eye [87].
Generally for ophthalmic formulations, particles ≤ 500 nm are indicated for efficient vitreal mobility [88] and permeation through ocular barriers. Moreover, a size-dependent disposition of nanoparticles studied by Amrite et al. indicated that very small particles (20 nm) undergo rapid clearance from the periocular tissue as compared with the larger particles (200 nm and 2 μm) which are retained for longer periods of up to 2 months. Systemic clearance via periocular blood or lymphatic circulation was indicated as a probable reason for rapid clearance of small particles [83, 89]. Thus, > 20–200–500 nm may be considered an optimum size for ocular formulations. In our case, 50% of particles are ≤ 250 nm and 90% particles are below 530 nm, establishing the suitability of ATS-SLNs for effective ocular uptake. Further, no particles of size < 30 nm (frequency of 1.2% at 36 nm; Supplementary Fig. 2(a)) were observed. The micrometric granular pattern and perinuclear finer fluorescence observed presently in the ARPE-19 cell line studies using F-SLNs as discussed in “Cellular uptake” (Fig. 12) also confirm that probably SLNs prepared presently with sizes 200–500 nm reach the nuclear membrane while the bigger particles (observed as a granular pattern) remain on the outside of the cells.
Usually a zeta potential of ≥ ± 25 mV is recommended for achieving stable dispersions. ATS-SLNs prepared presently by us, however, had a near neutral charge (zeta potential = − 2.65 mV) as shown in Supplementary Fig. 2(b) and were found to be stable with no significant change (p < 0.001) in particle size, TDC, and EE at 5 ± 3 °C for up to 1 year (“Stability studies”). The suitability of neutral nanoparticles for efficient retinal delivery of therapeutics with a capacity to evade reticuloendothelial system (RES) uptake is indicated in literature [90, 91].
Total drug content and entrapment efficiency
The drug content of the developed ATS-SLNs was 2.35 ± 0.05 mg/ml which was 94.00 ± 1.21% of what was originally incorporated (2.5 mg/ml) indicating an efficient production process.
A sufficiently high entrapment efficiency of 73.1 ± 1.52% (n = 6) was obtained.
In vitro release
The drug release profile of ATS-SLNs through dialysis membrane at 37 ± 0.5 °C (Fig. 4) showed a prolonged release with only 58.45% drug being released up to 96 h. Free drug on the other hand was released completely (100%) within 20 h. Fitting of release data to the various mathematical models like zero-order, first-order, Higuchi, and Korsmeyer–Peppas models indicated a first-order drug release (r2 = 0.986) pattern of ATS-SLNs. Higuchi release model (r2 = 0.932) was best fitted for ATS-SLNs at all the time points, indicating that drug release occurs by diffusion [92]. The latter was confirmed by the release exponent value (n) of 0.264, observed from the Korsmeyer–Peppas model indicating Fickian diffusion of ATS from ATS-SLNs. An almost 10% release observed at the first time point (15 min) is attributable to the unentrapped drug (~ 26%) in ATS-SLN dispersion.
FTIR, DSC, and XRD studies
FTIR
The FTIR spectra for blank SLNs and ATS-SLNs along with its various components are shown in Fig. 5. ATS showed intense absorption bands at 3363 cm−1 (O-H stretch), 3246 cm−1 (aromatic N-H stretch), 1650 cm−1 (aromatic C=O stretch), 1431 cm−1 (C-F aromatic stretch), 1315 cm−1 (C-O stretch of carboxylate group), 1217 cm−1 (C-N stretching of amide), and 695 cm−1 (aromatic out of plane bend), respectively [93].
Compritol® 888 ATO exhibited characteristic peaks at 2918 cm−1 and 2851 cm−1 (alkanes stretch) and 1741 cm−1 (C=O ester stretch). In the FTIR spectra of ATS-SLNs, peaks corresponding to ATS disappeared indicating its efficient entrapment in the lipid matrix, while the peaks corresponding to 2918 cm−1 (alkane stretch) and 2851 cm−1 (seen in Compritol® 888 ATO and P 90H) respectively are observable in both blank and ATS-SLNs. A peak corresponding to 1107 cm−1 for P 188 (1111 cm−1) representing C-O bond stretch [94] was observed for both blank and ATS-SLNs. This observation indicates that P 188 forms a layer on the surface of developed particles. The similarity of the FTIR spectra obtained for drug-loaded SLNs to that exhibited by blank SLNs, reconfirms efficient encapsulation of ATS within the lipidic core of developed SLNs.
DSC
Melting endotherm of ATS, corresponding to its melting point appeared at 164.81 °C (134.4 J/g), and Compritol® 888 ATO also showed a sharp peak at 73.1 °C again corresponding to its melting point, with an enthalpy of 109.3 J/g (Fig. 6). ATS-SLNs showed a broad endothermic shift to 86.93 °C and a significantly lowered heat flow of 15.03 J/g (Fig. 6), indicating incorporation of ATS into the lipid matrix.
Lower enthalpy for ATS-SLNs versus pure lipid indicates a reduction in particle size. Shift and broadening of endothermic peak of PEG 400 at 102.69 to 92.09 °C in blank SLNs with lower enthalpy (26.45 to 21.50 J/g) indicates interaction of PEG 400 with the lipid matrix. However, the peak corresponding to PEG 400 disappears completely in ATS-SLNs. This could mean that PEG effectively solubilizes ATS and helps in its incorporation within the lipid matrix of SLNs.
XRD
Powder X-ray diffraction study of pure drug (ATS) and lyophilized ATS-SLN formulation was performed to confirm the amorphous or crystalline nature of SLNs. ATS exhibited characteristic peaks between 2θ of 6.1 and 48.1 (Fig. 7), while these peaks disappeared in the XRD pattern of lyophilized ATS-SLN formulation, indicating loss of ordered lipid matrix [95] and the amorphousness of the formulation. Presence of some broad and diffuse peaks especially those corresponding to P 188 and P 90H were however observed as expected because P 188 covers the surface of the particles.
Stability studies
Stability studies under refrigerated conditions
No significant change (p < 0.001) in entrapment efficiency, total drug content, and particle size (except at 12 months) of ATS-SLNs was observed upon storage under refrigeration for 12 months, confirming their long-term stability (Table 5). TDC of ATS-SUS was however reduced to almost half (45.5%) at 12 months even under refrigerated condition. The significant improvement (13.62 times) in stability of ATS highlights importance of its incorporation into SLNs.
Table 5 Stability study at 5 ± 3 °C (n = 3) The SLN dispersion was also found stable to lyophilization (without cryoprotectant) with an insignificant (10–20 nm) change in particle size following redispersion of lyophilized formulation. Lyophilization usually results in an increase in size (100–200 nm) on reconstitution [96]. The lower tendency of present formulation to form aggregates during lyophilization may be due to the presence of 4% P 188, which completely covers the SLNs and thus stabilizes them. P 188 is reported to provide a stabilizing coat (outer shell) to SLNs [70].
Photostability studies
Total drug content of ATS-SLNs did not change significantly (p < 0.05; Table 6) before and after exposure to UV light during photostability studies, as per ICH guidelines, in an amber glass vial as well as clear glass vial. ATS-SUS however showed a significant (p < 0.05) drug loss (~ 30%) upon UV exposure. ATS is reported to undergo photooxidation especially at the pyrrole ring in its structure [31]. Protective shield provided by the enclosure within the lipid matrix of SLNs coupled by the anti-oxidant property of P 90H [74] and PEG 400 [97] may be responsible for protection of ATS against photodegradation.
Table 6 Photostability of ATS-SLNs and ATS-SUS (n = 3) Comprehensive testing as ocular drops
pH and osmolarity
The pH and osmolarity of ATS-SLN dispersion was 6.85 ± 0.5 and 210 ± 4.5 mOsm/l, respectively. Ocular drops with pH significantly different from tears (7.2) can elicit increased lacrimation due to irritation and pain. This can wash off and dilute the instilled drug from the eye fornix, resulting in a poor bioavailability. pH 7.2 ± 0.2 is defined as an optimum pH for maximum comfort in ophthalmic preparations [98]. The pH of the developed formulation was near neutral 6.85 ± 0.5 and did not require addition of any buffering agent.
Normal osmolarity of tears is 290–300 mOsm/l [99]. Hypotonic solution as obtained presently for ATS-SLNs (210 ± 4.5 mOsm/l) is advocated to be more suitable for ocular delivery in comparison with hypertonic or isotonic solutions [100]. Evaporation from the tear film tends to increase the osmolarity of the applied solution, and hyperosmotic drops can damage the ocular surface epithelia [79].
Refractive index and viscosity
Refractive index of ATS-SLNs (1.36) was found close to that of water (1.33) indicating that the developed SLN formulation would be appropriate for ocular use. Furthermore, for minimum interference with vision, a refractive index close to that of ocular tissues (1.34–1.41) as obtained presently is a desirable feature [101].
Optimal viscosity (ῂ) recommended for ocular drops is ≤ 20 cP. Higher values may result in reflex tearing and blinking in order to regain the original viscosity of the lacrimal fluid (1.05–5.97 cP). The viscosity for ATS-SLNs dispersion was 8.12 cP. The latter will not induce any excessive blinking or tearing while simultaneously retaining the dispersion on the surface of the eye for a longer period.
Stability upon sterilization
The developed ATS-SLNs were stable on autoclaving with no significant change (p < 0.05) in entrapment efficiency and particle size (Table 7). Sterilization is an important consideration in ocular delivery. Terminal sterilization is usually preferred as other methods involve post-sterilization handling, which requires trained personnel and aseptic handling, both of which add to the production cost. The achieved autoclavability of the developed system could be due to the selected components, viz. P 188, P90H, and PEG 400. These components change their performance with temperature and hence are harmonious to steam sterilization [102]. PEG being a plasticizer increases the rigidity of the system facilitating stability to autoclaving and resists gelation [80]. Lipidic particles are established to be physically stable to autoclaving conditions. Capacity to resist change in particle size and entrapment efficiency after autoclaving is especially reported for P 188 [103] and other Phospholipon-based SLNs [35]. SLNs are anticipated to melt during autoclaving followed by their recrystallization upon cooling [104, 105].
Table 7 Parameters before and after autoclaving (n = 3) Sterility testing
The developed and autoclaved blank formulation did not show any growth of fungus and bacteria until 14 days and were found to be sterile. The positive control and validation test confirmed the suitability of media and absence of any inhibitory activity of the formulation.
Corneal permeability studies
ATS-SLNs showed a significant improvement in apparent permeation coefficient (Papp) (2.2-fold), total amount permeated (1.6-fold), and percentage drug permeated (1.8-fold) at 4 h (Fig. 8) as compared with aqueous suspension of free ATS taken as control (Supplementary Table 3). Steady-state flux value increased by 2.5 times in comparison with ATS-SUS. ATS-SLNs showed significantly greater percentage permeation (Fig. 8) than ATS-SUS, at all times (p < 0.05).
The near normal corneal hydration (75–80%) confirmed that the ATS-SLNs did not damage the corneal endothelium or epithelium [106].
Since the target tissue for AMD is the macula, which is part of the retina, the topically applied drug should traverse the cornea and aqueous and vitreous humor to reach the retina. Corneal epithelium (which consists of several layers of cells and tight junctions created by cell adhesion proteins) acts as a major barrier to the drug entry into the eye. Significant improvement in flux (2.5 times) and total amount of ATS permeated (3.33 μg/min/cm2; 584 μg) when applied as ATS-SLNs versus ATS-SUS (1.33 μg/min/cm2; 373 μg) indicate improved permeation, attributed to the nanosize (256 nm) and composition of SLNs. Intercellular pore size of corneal epithelium is in the range of 200–300 nm, indicating the feasibility of paracellular transport of developed ATS-SLNs. Since the outermost (6–7 cells thick) epithelial layers of the cornea are lipophilic in nature, so free ATS which is also lipophilic showed significant permeation even when applied as ATS-SUS.
It may be noted that the ATS-SUS was prepared in 0.2% w/v sodium carboxymethyl cellulose used as a dispersing agent, and the latter has a strong mucoadhesive power which will result in prolonged retention of ATS-SUS in cul-de-sac of the eye [107].
Establishing safety of ATS-SLNs
Cytotoxicity studies
No statistically significant (p > 0.05) cytotoxicity of ATS-SLNs was observed (Supplementary Fig. 3) when administered to HCLE (at concentrations 1.5, 3, and 6 μg/ml); R28 (at concentrations 1.5 and 3 μg/ml); RCE (at concentrations 1, 100, and 1000 ng/ml); and ARPE-19 (1, 100, and 1000 ng/ml) cell lines after incubation for 24 h.
However, statistically significant (p < 0.01) cell viability loss was found at a high concentration of 6 μg/ml of ATS-SLNs in R28 cell lines. It may however be noted that the test concentration of 6 μg/ml is much more than the maximum concentration (Table 8; pharmacokinetic study discussed subsequently) of drug achieved in vivo, in aqueous (1.11 ± 0.16 μg/ml) and vitreous humor (1.43 ± 0.22 μg/ml), respectively, following topical administration.
Table 8 Pharmacokinetic parameters of ATS-SLNs and ATS-SUS following topical administration (n = 4) In vivo safety studies
The score for both (i) acute dermal irritation/corrosion study [108] (Supplementary Table 4) and (ii) acute eye irritation [109] (Supplementary Table 5) was 0, thus demonstrating a non-irritant nature of developed ATS-SLNs and confirming them to be safe for ocular use.
Repeat instillation study was performed in view of the fact that AMD and related pathologies require lifelong treatment and will need daily instillation of statin formulations for effective control of the disease. Similar studies have been reported by us earlier [35, 110]. The score obtained from this study was also 0 (Supplementary Table 6) and proves the system to be safe for repetitive ocular use.
Similarly aggressive therapy, viz. chronic repeat instillation (5 times at 5-min interval), for a period of 1 week was also evaluated, and the SLN formulation was again found to be safe (Supplementary Table 7) for chronic ocular use. Safety was also expected as all the ingredients employed for preparing the SLN formulation are biodegradable, biocompatible, and safe for ocular use [66] at the employed concentrations.
Ocular tolerance evaluation
Corneal, retinal, and conjunctival cross sections post ATS-SLN administration were observed microscopically to investigate its influence on cell structure and tissue integrity. Results confirm that application of ATS-SLNs to the eye did not compromise tissue integrity in anyway. No inflammation or damage was observed in the retina and sclera. The developed formulation left the tissue structure and integrity visibly unaffected (Supplementary Fig. 4). Results confirm good ocular biocompatibility of the developed formulation.
Cytotoxicity studies on corneal and retinal cell lines confirmed the biocompatibility of the developed system even for exposures as long as 24 h. Corneal hydration rates obtained (≥ 80%) in the ex vivo corneal permeation studies also match with those (76–80%) claimed to be normal [106], establishing safety of the formulation. Furthermore, the developed SLNs were also evaluated for the ocular tolerance in rabbits. It is reported in literature that the rabbit eye is more sensitive than the human eye and requires a longer epithelial repair time [111]. Thus, it is rational to expect an even better tolerance by the human eye [71] for the developed SLN formulation. The three-tier (in vitro, ex vivo, and in vivo) data obtained presently helps to conclude safety of the developed formulation.
Residence time
Optical images of fluid withdrawn from corneal surface post instillation of F-SLN drops showed (Fig. 9) fluorescence and/or intact fluorescent SLNs up to 7 h, while corresponding free fluorescein solution (F-SOL) failed to exhibit any fluorescence within 1.5 h of topical instillation. The longer residence of SLNs on the eye may be attributed to their mucus penetration effects. Mucus is the first protective barrier which checks entry of any foreign particles including bacteria into the eye, by entrapping them into luminal mucus layer (LML). The latter is rapidly cleared, preventing contact of such particles with the corneal epithelium. It may thus be said that mucoadhesive particles including nanoparticles will be eliminated from the eye as they are largely immobilized in the LML while mucus-penetrating particles quickly pass through the LML to reach the underlying adherent mucus which is cleared slowly. P 188–based nanosized mucus-penetrating particles (MPPs) of loterprednoletabonate (LE) showed higher therapeutic drug levels in the posterior eye in comparison with conventional nanoparticles of LE [112]. Particles developed by us contain PEG 400 in addition to P 188, and both these polymers have been established as effective mucopenetrating agents [113]. Low molecular weight PEGs are especially studied for their mucus-penetrating effects [114]. P 188 (poly ethylene glycol (PEG)-poly propylene oxide (PPO)-PEG; known as pluronics) can coat lipidic particle surface by adsorption of the hydrophobic PPO segments, leaving a dense brush of uncharged, hydrophilic segments protruding from the particle surface [80]. The latter can help these particles to swim through the mucus and reach the corneal surface. Since the particles were observed on the corneal surface up to 7 h, hence, it may be said that they penetrated the mucus layer to reach and interact with the corneal surface.
Cellular uptake
At 2-h post-incubation of F-SLNs (Fig. 10a), at a concentration of 3 μg/ml with ARPE-19 cells, a micrometric granular pattern and perinuclear finer fluorescence were observed around and in the cells. Free fluorescein solution (Fig. 10b) treatment did not show fluorescence in or near the cells. Entry of smaller SLNs (50–100 nm, approx. 10% of total) through the cell membrane to reach the nuclear membrane could explain the perinuclear fluorescence. The granular pattern on the surface of the cells could be due to the bigger particles (> 100 nm; 90%) which do not permeate (Supplementary Fig. 2 particle size distribution) easily. These particles, however, either (i) may undergo erosion to smaller particles before their uptake or (ii) may release ATS which can permeate into cells in association with smaller particles. All particles however probably produce some permeability changes. This fact is supported by an enhanced UV-induced apoptosis (as discussed subsequently in the apoptosis study) observed with blank SLNs.
Effect of ATS-SLNs on apoptosis
This study was designed to assess if ATS-SLNs exert apoptosis and hence induce anti-angiogenesis in the retinal and corneal cells. The latter is the proposed mechanism of action of commonly used AMD medication, viz. the anti-VEGF antibodies. Anti-angiogenic effects of statins were mostly achieved at high concentrations (> 0.1 μmol/l atorvastatin) [123]. UV-irradiated ARPE-19 cells showed a viability loss of about 73% with respect to non-irradiated cells (Fig. 11). This was increased to approx. 93% upon treatment with blank SLNs (100 and 1000 ng/ml). However, the effect was completely abrogated and there was a trend (even if not significant) of ATS-SLNs to counteract the toxic effect of UV. Free ATS (ATS-SUS) did not show any effect both on viability and on apoptosis (Fig. 12). UV-irradiated RCE cells showed a viability loss of about 85% with respect to non-irradiated cells, while no differences were seen following treatments (data not shown). However, no change in viability was observed when antimycin was used instead of UV irradiation as an apoptotic stimulus, both in ARPE-19 and in RCE cells (data not shown).
Apoptosis was demonstrated to be responsible for UV-induced viability loss by the time-lapse (Fig. 12), FACS (Supplementary Fig. 5), and cytochrome C release (Supplementary Fig. 6) analyses. Time-lapse experiments showed the ability of blank SLNs to enhance the apoptotic effect of UV at times beyond 24 h. SLNs probably produce some permeability changes in ARPE-19 cells, which enhance UV-induced apoptosis. It is reported that opening of permeability transition pore (PTP) in a mitochondrial cell membrane leads to apoptosis [115]. Induced apoptotic effect is however counteracted in the ATS-SLN group. ATS was reported to inhibit PKC inhibitor–induced apoptosis, in adult rat cardiac myocytes [116,117,118].
This experiment indicates that ATS has no apoptotic effect on ARPE-19 cells (Figs. 11 and 12) and RCE cells.
More detailed investigations, which were out of the scope of presently planned studies, are thus indicated to establish the mechanisms by which ATS can treat AMD symptoms. The anti-inflammatory and anti-oxidant effects are also highly indicated.
Pharmacokinetic study
The concentration–time profiles and corresponding pharmacokinetic parameters of ATS-SLN and ATS-SUS after topical administration in aqueous and vitreous humor are shown in Fig. 13 and Table 8, respectively. A higher Cmax (1.6-fold) and AUC (7.0 fold) for ATS-SLNs with respect to the ATS-SUS was noted in aqueous humor. Similarly, 3.0-fold and 11.7-fold higher effects in vitreous humor were observed for Cmax and AUC, respectively. Significantly higher ocular delivery potential of ATS-SLNs in comparison with free ATS may be attributed to improved transcorneal and conjunctival uptake of ATS-SLNs because of their nanosize and penetration enhancing effect of Compritol® 888 ATO and P 188 [69]. Conjunctival pathway is now identified as the key pathway for posterior eye delivery [52]. Prolonged precorneal retention, mucus penetration and improved permeation, and probable p-gp efflux inhibition due to the presence of PEG 400 and P 188 in the ATS-SLNs are the several reasons assigned to improved ocular bioavailability observed with the latter. Similar improvements in concentration of cyclosporine A [119] and gatifloxacin [120] were reported in aqueous and vitreous humor following topical administration of their respectively loaded SLNs.
Peak effect was obtained within 60 min of instillation of the last drop of SLNs (five 30-μl drops of ATS-SLNs were instilled into each eye at 5-min intervals) while free ATS showed a peak effect at 30 min for aqueous humor and 60 min for vitreous humor. Early Tmax of ATS-SUS may be due to the strong mucoadhesive nature of sodium carboxymethyl cellulose used as suspending/dispersing agent and the intrinsic lipophilic nature of ATS (log P = 4.41). However, a significantly higher Cmax and a sustained effect (AUC 700% and 1170% in aqueous and vitreous humor) of up to 48 h (versus 6 h for ATS-SUS) observed for ATS-SLNs as also indicated by the extended MRT of 3–3.5-fold, demonstrate the effectiveness of ATS-SLNs. Furthermore, elimination rate constant (Kel) of developed SLN formulation was found to decrease by 3.5 times re-establishing a prolonged effect.
The protective covering provided by SLNs to ATS not only improves its stability to oxidation and photodegradation but probably also prevents its in vivo metabolism [29]. T1/2 of ATS in plasma is reported to be 14 h. However, ATS-SUS exhibited a T1/2 of 2.6 h and 4.7 h respectively in aqueous and vitreous humor. Anti-fungals like ketoconazole, fluconazole, and amphotericin B are also reported to show a higher T1/2 in plasma versus that exhibited in ocular fluids (as the T1/2 depends on the dose, dosage form, and route of administration) [121]. However, the T1/2 was significantly increased (by 3–4 times) to 9.2 and 14.4 h in aqueous and vitreous humor, respectively, following administration of ATS as ATS-SLNs. Furthermore, a sustained concentration of about 250 ng was maintained in the vitreous humor from 12 to 48 h while the value was negligibly low at ≥ 6 h with ATS-SUS. Since the macula is the major target for control of AMD, hence, higher and better sustained concentration of ATS in vitreous following topical application of ATS-SLNs is a highly promising indication. Vitreous humor is formed and removed at a much slower rate (0.45 μg/day) than aqueous humor (2.4 ± 0.6 μl/min), such that it may be assumed that the limiting step for any drug delivery system is to reach the vitreous humor and once that is achieved, it may accumulate in the vitreous humor to a larger extent than in the aqueous humor [51]. However, viscous nature of the vitreous humor can at times limit the access of the carrier system to the posterior part of the eye including the retina and macula. SLNs prepared by us comprise PEG and P 188, both of which are expected to help these SLNs to stream through the vitreous humor due to their neutral surface and mucus-penetrating nature [112].
Literature demonstrates that only 50–80 ng/ml of ATS is found in human plasma and/or serum after oral administration of 40 mg of ATS [122]. For lipophilic drugs, it is indicated that only one-third of the drug in plasma can reach the aqueous and vitreous humor of the eye. Based on this, not more than or equal to 30 ng/ml of ATS is expected to reach the ocular fluids following its oral administration. In contrast, topical administration of 150 μl (equivalent to 375 μg ATS) of ATS-SLNs administered presently to rabbits achieved 1430 ng/ml of ATS in vitreous humor and 1110 ng/ml in aqueous humor which is around 30 times higher than the reported plasma concentrations or 48 times more than the expected ocular concentration. Localized concentration of ATS in vitreous humor will ensure minimal systemic side effects, viz. constipation, flatulence, dyspepsia, and abdominal pain associated with use of ATS. Furthermore, incidence of severe rhabdomyolysis (which at times may be fatal) in a significant patient population leads to discontinuation of oral ATS therapy. Such side effects will be significantly reduced while better therapeutics will be achieved following ocular application of ATS-SLNs.
Proof-of-concept studies with F-SLNs
Histological sections showed diffuse fluorescence in the vitreous humor, retina, sclera, and choroid of the rat eye, post single-drop instillation of the fluorescein sodium–labeled SLNs. Intact particles were also observed in these tissues as indicated by white arrows in Fig. 14.
Rows 1, 2, and 3 show the sections of the cornea, vitreous humor, and posterior tissues prepared 0.5-h, 1-h, and 2-h post-application, respectively. Red arrows indicate different layers of tissues and white arrows show presence of intact and fluorescing SLNs.
A representative illustration of confocal microscopy (Fig. 15), after 1-h application, substantiates penetration potential of the developed SLN formulation. Significant higher fluorescence was observed in the cornea, sclera, choroid, and retina including the RPE and vitreous humor in comparison with free fluorescein.
It is generally observed that a topically dosed drug can transport to the posterior segment from ocular surface through (1) the transcorneal route which can be divided further into (a) transvitreous route—where drug diffuses through the cornea, enters the vitreous cavity, and distributes to the back of the eye; (b) the uvea–scleral route where drug diffuses through the cornea, penetrates the aqueous humor, and continues through the uvea–sclera where it can gain access to the choroid and retina; and the (2) periocular route (conjunctival uptake), where diffusion occurs around the sclera and drugs are absorbed through the sclera [84, 120]. Presence of intact particles observed in the sclera, cornea, retina, and vitreous humor indicates that transport of developed SLNs occurs not only through corneal pathways (Fig. 14) but also via conjunctival/scleral route due to their small size and charge free surface. Higher permeation of ATS-SLNs may also be attributed to PEG-modified surface (both PEG 400 and PEG blocks of P 188) of developed SLNs. The latter have a capability to solubilize cell membrane due to their solubility in both polar and non-polar materials [107]. Presence of ATS-SLNs (even after 6 h) at precorneal site (Fig. 9) indicates their prolonged retention and/or mucus-penetrating nature. Presence of SLNs in the STF withdrawn by washing the rabbit corneal surface may be attributed to the forced blinking (5–6) of the rabbit eye induced by us prior to each sampling point, as this will detach the mucus entangled particles adhering to the corneal surface. Longer retention of presently developed nanosystem was also confirmed by presence of significant fluorescence in the cornea even after 2 h of administration (Fig. 15). Furthermore, the capacity of developed SLNs to reach the vitreous humor, retina, and RPE in intact form (as seen from fluorescence and confocal microscopy) is complemented with higher achieved therapeutic concentration of ATS (as seen from vitreous pharmacokinetic study). Cellular uptake of these particles was also confirmed in the in vitro studies (Fig. 10).