Investigation of Physical Properties of a Polycaprolactone Dermal Filler when Mixed with Lidocaine and Lidocaine/Epinephrine
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In esthetic treatments with dermal fillers, increasing numbers of physicians are using the technique of mixing an anesthetic agent into the dermal filler before treatment to increase the comfort of the patients. This study aimed at evaluating the effects on the physical properties of a polycaprolactone (PCL)-based dermal filler after mixing with lidocaine.
A range of 2.0% lidocaine and 2.0% lidocaine/epinephrine concentrations was mixed with the PCL dermal filler to evaluate the changes in dynamic viscosity and elasticity, extrusion force, pH, and needle jam rates. The number of passes back to forth for optimal homogeneity of lidocaine and PCL dermal filler was determined.
With 15 mixing strokes the lidocaine solution can effectively be mixed into dermal filler resulting in a homogenous blend. The viscosity, elasticity, and the extrusion force decrease with increasing lidocaine volume. The viscosity and elasticity of the dermal filler is sufficient to keep the PCL microspheres in suspension. There were no needle jams. The pH of the PCL dermal filler mixed with lidocaine solution is equivalent to that of the original dermal filler.
It is concluded that mixing of lidocaine into the PCL-based dermal filler can safely be performed without harmful changes in the physical properties of the original dermal filler.
KeywordsCarboxymethylcellulose Dermal filler Dermatology Elasticity Esthetic treatment Lidocaine Polycaprolactone Viscosity
Polycaprolactone (PCL)-1 dermal filler (Ellansé™; AQTIS Medical, Utrecht, the Netherlands) is a soft tissue dermal filler based on PCL microspheres. The smooth and totally spherical-shaped PCL microspheres (25–50 μm) are homogenously suspended in a tailor-made aqueous carboxymethylcellulose (CMC) gel carrier.
PCL and CMC individually have an excellent and established biocompatibility profile and have been used successfully in numerous Conformité Européenne marked and US Food and Drug Administration approved medical devices, such as dermal fillers, oral and maxillofacial surgery, wound dressing and controlled drug delivery [1, 2, 3, 4, 5, 6].
PCL is a totally bioresorbable, nontoxic medical polymer and is attractive for use in medical devices because of its controlled and safe bioresorption process [7, 8, 9, 10, 11]. With 3H-labeled PCL and C14-labeled PCL implantation studies, it has been proved that PCL was completely excreted from the body [7, 8].
After treatment the CMC gel carrier is gradually resorbed by macrophages over a period of several weeks, during which the PCL microspheres will trigger a natural response of the human skin and stimulate a natural wound-healing process through neocollagenesis. The new collagen replaces the volume of the resorbed carrier. The microspheres are not phagocytosed because of their size and surface characteristics. The PCL microspheres are totally smooth and spherical shaped, which has been shown to be optimal for dermal fillers [12, 13]. The PCL dermal filler is indicated for deep dermal and subdermal implantation.
In 2007 Busso and Applebaum  published a report of their experiences in mixing a calcium hydroxylapatite-based dermal filler with lidocaine for use of the soft tissue filler in treatment of the hand. The result of mixing the two components is that the treatment is less painful to the patient than the conventional hand injection, and is characterized by less swelling and bruising, with minimal posttreatment downtime.
Increasing numbers of physicians are adopting and using this technique for mixing the PCL dermal filler with standard 2.0% lidocaine-hydrochloride (HCl) solutions, up to 0.19 mL of lidocaine with a 1.1 mL syringe of PCL dermal filler. Mixing 0.19 mL of 2.0% lidocaine solution with 1.1 mL of PCL dermal filler yields a 0.3% lidocaine concentration. This concentration is equivalent to that found in other soft tissue fillers, such as Restylane and Juvederm [15, 16]. The authors suggest that adding up to 0.3% of the anesthetic agent lidocaine to the PCL-based filler will not substantially affect its characteristics, confirming the usability of this mixture in clinical practice.
Materials and Methods
Study Purpose and Design
In this study the characterization of the physical properties of PCL dermal filler mixed with plain 2.0% lidocaine-HCl solutions and combined 2.0% lidocaine-HCl and epinephrine under various mixing condition is investigated.
A range of lidocaine and lidocaine with epinephrine concentrations was mixed with the PLC dermal filler to evaluate the changes in dynamic viscosity and elasticity, extrusion force, pH, and needle jam rates. Investigators also evaluated the mixtures at the front, middle, and back of each mixed syringe as a measure of mixing efficiency.
Materials and Equipment
For this study 1.1 mL syringes of the PCL-1 dermal filler were used. The usage of the PCL dermal filler in this study is representative of the entire product line as all the relevant product characteristics are identical throughout the entire product range. Testing was performed on three different commercial lots.
The 2.0% lidocaine solution was composed of anhydrous lidocaine-HCl (20 mg/mL) (Xylocaine 2.0%; Astra Zeneca BV, Zoetermeer, the Netherlands). The 2.0% lidocaine solution with epinephrine was composed of anhydrous lidocaine-HCl (20 mg/mL), epinephrine (5 μg/mL) (Xylocaine 2.0% with epinephrine; Astra Zeneca BV).
A rheometer (Haake RS-6000; Thermo Electron GmbH, Karlsruhe, Germany) was used to measure the dynamic viscosity and elasticity of the media. Rheology was evaluated with a titanium rotor, with a gap of 0.105 mm and tau (τ) of 5 Pa, over a frequency sweep of 0.1–10 Hz evaluated at 0.6 Hz. Extrusion force was measured by a material tester (model H1Ks; Tinius Olsen, Ltd., Salfords, Surrey, UK). Extrusion force was evaluated through a 27G¾ inch needle with an extension rate of 1 mL/min.
Media pH was measured using a pH meter with a probe (pH340I, and Sentix 41 probe, respectively; WTW, Weilheim, Germany). The pH was obtained by completely coating the glass bulb of the pH probe with media. The female-to-female Luer lock connectors used to connect the mixing and media syringes were from Baxa (rapid fill connector, ref. 13901; Bracknell, Berkshire, UK).
For the PCL-1 dermal filler, 1.1 mL syringes were mixed with one of four volumes of 2.0% lidocaine or 2.0% lidocaine with epinephrine solution: 0.05 mL (0.09% final lidocaine-HCl); 0.10 mL (0.17% final lidocaine-HCl); 0.14 mL (0.23% final lidocaine-HCl); 0.19 mL (0.30% final lidocaine-HCl).
Lidocaine and PCL dermal filler were mixed by alternately depressing the plungers on the mixing and media syringes. Each mixing stroke was composed of one complete compression of the dermal filler syringe push rod, followed by one complete compression of the mixing syringe push rod. Push rods were compressed firmly and quickly, at approximately two compressions per second.
Following mixing, the mixing syringe and Luer lock connector were removed and discarded, and the lidocaine/dermal filler mixture was recapped with the original media syringe cap. The dermal filler-lidocaine blends were tested between 15 min and 120 min after mixing with lidocaine.
Number of Passes Between Syringes Sufficient for Blending of Lidocaine with PCL Dermal Filler
The extrusion force was used to determine the number of passes between syringes needed for sufficient blending of lidocaine with the PCL dermal filler. With adequate mixing of the components the difference in viscosity across all regions of the syringe is minimal and the extrusion force profile is uniform from the front to the back of the syringe.
The difference in viscosity from the front to the back increased with increasing volume of lidocaine, suggesting that larger volumes of lidocaine required more mixing than small volumes. It also reflects a greater magnitude of change in physical properties with increasing concentration of lidocaine.
Dynamic Viscosity of PCL Dermal Filler Compared to PCL Dermal Filler with Lidocaine Mixtures with or without Epinephrine
Even at 0.23 mL of lidocaine solution blended with the PCL dermal filler, the CMC gel viscosity/elasticity was sufficient enough to keep the PCL microspheres in suspension in time (not shown).
Extrusion Forces of PCL Dermal Filler Compared to PCL Dermal Filler with Lidocaine
The extrusion forces of the PCL dermal filler mixed with lidocaine were lower than those of the PCL dermal filler alone. The average extrusion force decreased with the increase in volume of lidocaine added to the 1.1 mL PCL dermal filler syringe.
Differences in average extrusion force for PCL dermal filler mixed with lidocaine with and without epinephrine was not statistically significant for all volumes, suggesting that epinephrine had no effect on the extrusion force.
Incidence of Needle Jamming in PCL Dermal Filler Blended with Lidocaine with or without Epinephrine
Needle jamming may occur if there is a cluster of PCL microspheres in the CMC gel carrier.
No needle jams were observed in any of the extrusion tests, indicating optimal homogeneity and suspension of the PCL microspheres in the CMC gel carrier after mixing with lidocaine with or without epinephrine.
Elasticity and pH of PCL Dermal Filler Blended with Lidocaine Compared to PCL Dermal Filler without Lidocaine
The pH was between 7.1 and 7.2 for all tested samples.
Hand mixing lidocaine or lidocaine with epinephrine with the PCL dermal filler causes no significant changes to the physical properties of the original formulation. With 15 back-and-forth passes the anesthetic agent(s) can adequately be mixed into the gel resulting in a homogenous blend. The viscosity/elasticity of the gel in the PCL dermal filler mixed with 2.0% lidocaine with or without epinephrine is sufficient to keep the PCL microspheres in suspension even after 24 h. There were no needle jams, indicating that the PCL microspheres were homogenously suspended in the gel, even after mixing the dermal filler with the anesthetic agent. The pH values of the PCL dermal filler mixed with lidocaine with or without epinephrine are equivalent to those of the original dermal filler. The viscosity, elasticity, and the extrusion force of the dermal filler decrease with increasing lidocaine content. There was no statistically significant change in physical properties for lidocaine solutions with or without epinephrine. The changes in physical properties are identical for the entire product range.
Mixing a lidocaine solution with the dermal filler obviates the need for nerve blocks or local infiltration, thereby reducing the treatment times and prevents tissue distortion that may be caused by injecting local anesthetics. This may also positively affect the patients’ treatment experience and satisfaction. In addition, previous studies have shown that the addition of lidocaine to collagen-based dermal fillers resulted in less swelling and bruising , potentially due to the antihistaminergic effect of lidocaine on mast cells . Similar findings have been reported for hyaluronic acid-based dermal fillers mixed with lidocaine, also showing a reduction in swelling, erythema, and bruising [16, 19, 20, 21]. As lidocaine is suggested to decrease these side effects, this is also expected for the PCL-based dermal filler mixed with lidocaine.
The limitations of this study are that it does not investigate the influence of lidocaine and epinephrine on the clinical safety and performance of the PCL dermal filler, and the influence of the clinical anesthetic effect of lidocaine after mixing with the PCL dermal filler.
This study does not address a potential interaction of lidocaine or epinephrine with the components of the PCL dermal filler and its potential influence on anesthetic efficacy. It is expected that, because of its hydrophilicity, lidocaine will be situated in the aqueous (hydrophilic) CMC gel carrier. Predicted on the hydrophobicity of the nonporous PCL microspheres  no affinity is expected between lidocaine and PCL microspheres, and there will be no driving force of the lidocaine to migrate into the PCL microspheres.
This is supported by a study describing the release profile of lidocaine from PCL threads . PCL pellets were compounded with lidocaine and then extruded to obtain highly loaded threads. The lidocaine release profile showed a rapid release in the first hours and completed in a few days, indicating that there is no affinity or reaction between the PCL matrix and lidocaine.
It is not expected that lidocaine will bind or react with the CMC carrier, but is free to move and yield the desired anesthetic effect. CMC is a known time-release agent for lidocaine , and there are several commercial medical products available based on CMC gel and lidocaine as an anesthetic agent.
This study does not address the effect of the premixed anesthetic on the clinical efficacy of the PCL dermal filler. Physicians have reported no decrease in clinical efficacy after mixing the PCL dermal filler with lidocaine with or without epinephrine, as has also been reported for hyaluronic acid-based dermal fillers containing lidocaine (for review, see Smith and Cockerham ). Planned (pre)clinical studies with lidocaine premixed before treatment and lidocaine incorporated in the PCL dermal filler syringe itself are aimed at confirming this.
The advantages of mixing lidocaine with PCL dermal filler before treatment are lower viscosity and elasticity, lower extrusion force, providing a greater ease of molding, increased patient comfort, reduced need for nerve blocks and infiltration anesthesia, which may be attractive for both physicians and patients.
The work was performed at the research facility of AQTIS Medical in Utrecht, the Netherlands. Dr. Marijnissen-Hofsté is the guarantor for this article, and takes responsibility for the integrity of the work as a whole.
Conflict of interest
Dr. de Melo is an advisor of AQTIS Medical, and has received consultancy and speaking fees from the company. Dr. Marijnissen-Hofsté is an employee of AQTIS Medical.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
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