Skip to main content
Log in

Roles of cryo/thermal strength for redispersibility of drug nanocrystals: a representative study with andrographolide

  • Research Article
  • Published:
Archives of Pharmacal Research Aims and scope Submit manuscript

Abstract

Due to limited understanding about the effect of cryo/thermal strength from drying process on the redispersibility of drug nanocrystals, the impact of the different type and concentration of stabilizers and matrix formers on the redispersibility of nanocrystals were systematically investigated. Andro nanosuspensions were transformed into Andro nanocrystals (Andro-NC) via different drying process. The results demonstrated that the redispersibility of Andro-NC at the aggressive cryo-strength (meant higher freezing rate) was more excellent than those at conservative and moderate condition. Compared to the thermal stress from drying, the employed amount and type of stabilizers more dramatically affected the redispersibility of Andro-NCP during lyophilization. The HPMC-sucrose and HPMC-sorbitol system achieved excellent performance that protected Andro-NC from crystal growth during lyophilization. During spray-drying, the impacts of types and amounts of stabilizers on the redispersibility of Andro-NCP were more significant compared to those induced by the thermal stress conditions. The polymers HPMC, PVPK30 and MCCS with high Tg played an outstanding role in preventing the Andro-NCP from breakage during spray-drying, due to the firmly steric barrier effect of polymeric stabilizers. It is concluded that Andro-NCP is subjected to agglomeration or crystal growth due to cryo/thermal stresses during drying. The polymeric stabilizers are more effective to protect Andro-NCP from the cryo/thermal damage during solidification process, which behaved strong surface adsorption and high glass transition property at different solidification stress.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11
Fig. 12

Similar content being viewed by others

References

  • Abdelwahed W, Degobert G, Stainmesse S, Fessi H (2006) Freeze-drying of nanoparticles: formulation, process and storage considerations. Adv Drug Deliv Rev 58:1688–1713

    Article  CAS  PubMed  Google Scholar 

  • Allison SD, Molina MC, Anchordoquy TJ (2000) Stabilization of lipid/DNA complexes during the freezing step of the lyophilization process: the particle isolation hypothesis. Biochim Biophys Acta 1468:127–138

    Article  CAS  PubMed  Google Scholar 

  • Carpenter JF, Crowe JH (1989) An infrared spectroscopic study of the interactions of carbohydrates with dried proteins. Biochemistry 28:3916–3922

    Article  CAS  PubMed  Google Scholar 

  • Chaubal MV, Popescu C (2008) Conversion of nanosuspensions into dry powders by spray-drying: a case study. Pharm Res 25:2302–2308

    Article  CAS  PubMed  Google Scholar 

  • Chellampillai B, Pawar AP (2011) Improved bioavailability of orally administered andrographolide from pH-sensitive nanoparticles. Eur J Drug Metab Pharm 35:123–129

    Article  CAS  Google Scholar 

  • Figueroa CE, Bose S (2013) Spray granulation: importance of process parameters on in vitro and in vivo behavior of dried nanosuspensions. Eur J Pharm Biopharm 85:1046–1055

    Article  CAS  PubMed  Google Scholar 

  • Gao L, Liu G, Ma J, Wang X, Zhou L, Li X (2012) Drug nanocrystals: in vivo performances. J Control Release 160:418–430

    Article  CAS  PubMed  Google Scholar 

  • Gu Y, Ma J, Liu Y, Chen B, Yao S (2007) Determination of andrographolide in human plasma by high-performance liquid chromatography/mass spectrometry. J Chromatogr B 854:328–331

    Article  CAS  Google Scholar 

  • Ige PP, Baria RK, Gattani SG (2013) Fabrication of fenofibrate nanocrystals by probe sonication method for enhancement of dissolution rate and oral bioavailability. Colloids Surf B 108:366–373

    Article  CAS  Google Scholar 

  • Iskandar F, Gradon L, Okuyama K (2003) Control of morphology of nanostructured particles prepared by the spray dying of a nanoparticle sol. J Colloid Interface Sci 265:296–303

    Article  CAS  PubMed  Google Scholar 

  • Jinno JI, Kamada N, Miyake M, Yamada K, Mukai T, Odomi M, Toguchi H, Liversidge GG, Higaki K, Kimura T (2006) Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J Control Release 111:56–64

    Article  CAS  PubMed  Google Scholar 

  • Kim S, Lee J (2010) Effective polymeric dispersants for vacuum, convection and freeze-drying of drug nanosuspensions. Int J Pharm 397:218–224

    Article  CAS  PubMed  Google Scholar 

  • Kurozawa LE, Park KJ, Hubinger MD (2009) Effect of maltodextrin and gum arabic on water sorption and glass transition temperature of spray dried chicken meat hydrolysate protein. J Food Eng 91:287–296

    Article  CAS  Google Scholar 

  • Lai F, Pini E, Angioni G, Manca ML, Perricci J, Sinico C, Fadda AM (2011) Nanocrystals as tool to improve piroxicam dissolution rate in novel orally disintegrating tablets. Eur J Pharm Biopharm 9:552–558

    Article  Google Scholar 

  • Lee J (2003) Drug nano-and microparticles processed into solid dosage forms: physical properties. J Pharm Sci 92:2057–2068

    Article  CAS  PubMed  Google Scholar 

  • Merisko-Liversidge E, Liversidge GG (2011) Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology. Adv Drug Deliver Rev 63:427–440

    Article  CAS  Google Scholar 

  • Molina MC, Armstrong TK, Zhang Y, Patel MM, Lentz YK, Anchordoquy TJ (2004) The stability of lyophilized lipid/DNA complexes during prolonged storage. J Pharm Sci 93(9):2259–2273

    Article  CAS  PubMed  Google Scholar 

  • Niwa T, Danjo K (2013) Design of self-dispersible dry nanosuspension through wet milling and spray freeze-drying for poorly water-soluble drugs. Eur J Pharm Sci 50:272–281

    Article  CAS  PubMed  Google Scholar 

  • Panossian A, Hovhannisyan A, Mamikonyan G, Abrahamian H, Hambardzumyan E, Gabrielian E, Goukasova G, Wikman G, Wagner H (2000) Pharmacokinetic and oral bioavailability of andrographolide from andrographis paniculata fixed combination Kan Jang in rats and human. Phytomedicine 7:351–364

    Article  CAS  PubMed  Google Scholar 

  • Pawar VK, Singh Y, Meher JG, Gupta S, Chourasia MK (2014) Engineered nanocrystal technology: in vivo fate, targeting and applications in drug delivery. J Control Release 83:51–66

    Article  Google Scholar 

  • Rabinow BE (2004) Nanosuspensions in drug delivery. Nat Rev Drug Discov 3:785–796

    Article  CAS  PubMed  Google Scholar 

  • Syamaladevia RM, Sablania SS, Tang J, Powers J, Swanson BG (2010) Water sorption and glass transition temperatures in red raspberry (Rubus idaeus). Thermochim Acta 503:90–96

    Article  Google Scholar 

  • Van Eerdenbrugh B, Froyen L, Martens JA, Blaton N, Augustijns P, Brewster M, Van den Mooter G (2007) Characterization of physicochemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling. Int J Pharm 338:198–206

    Article  PubMed  Google Scholar 

  • Van Eerdenbrugh B, Vercruysse S, Martens Johan A, Vermant J, Froyen L, Van Humbeeck J, Van den Mooter G, Augustijns P (2008) Microcrystallinel-celluose, a useful alternative for sucrose as a matrix former during freeze-drying of drug nanosuspensions-a case study with itraconazole. Eur J Pharm Biopharm 70:590–596

    Article  PubMed  Google Scholar 

  • Verma S, Kumar S, Gokhale R, Burgess DJ (2011) Physical stability of nanosuspensions: investigation of the role of stabilizers on ostwald ripening. Int J Pharm 406(1–2):145–152

    Article  CAS  PubMed  Google Scholar 

  • Wang T, Liu B, Zhang W, Wilson B, Hong JS (2004) Andrographolide reduces inflammation-mediate ddopaminergic neurodegeneration in mesencephalic neuron-glia cultures by inhibiting microglial activation. J Pharmacol Exp Therapeut 308:975–983

    Article  CAS  Google Scholar 

  • Ye L, Wang T, Tang L, Liu W, Yang Z, Zhou J, Zheng Z, Cai Z, Hu M, Liu Z (2011) Poor oral bioavailability of a promising anticancer agent andrographolide is due to extensive metabolism and efflux by P-glycoprotein. J Pharm Sci 100:5007–5017

    Article  CAS  PubMed  Google Scholar 

  • Yue P, Wang Y, Wan J, Wu Z, Hu P, Zheng Q, Yuan H, Yang M (2012) The research progress of preparation methods of solid nanocrystal delivery system. Acta Pharm Sin 47(9):1120–1127

    CAS  Google Scholar 

  • Yue P, Li G, Dan J, Wu Z, Wang C, Zhu W, Yang M (2014) Study on formability of solid nanosuspensions during solidification: II novel roles of freezing stress and cryoprotectant property. Int J Pharm 475(1–2):35–48

    Article  CAS  PubMed  Google Scholar 

  • Yue P, Xiao M, Xie Y, Ma Y, Guan Y, Wu Z, Hu P, Wang Y (2015) The roles of vitrification of stabilizers/matrix formers for the redispersibility of drug nanocrystals after solidification: a case study. AAPS Pharm Sci Tech. doi:10.1208/s12249-015-0461-3

    Google Scholar 

Download references

Acknowledgments

The authors would like to acknowledge the financial support from the Scientific Research Foundation for the National Natural Science Foundation of China (No. 81560656 and the Natural Science Found of Jiangxi Province (No. 20122BAB215038).

Conflict of interest

The authors declare that there are no conflicts of interest.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to PengFei Yue or Qin Zheng.

Additional information

YuanBiao Xie and YueQin Ma contributed to the work equally as joint first authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xie, Y., Ma, Y., Xu, J. et al. Roles of cryo/thermal strength for redispersibility of drug nanocrystals: a representative study with andrographolide. Arch. Pharm. Res. 39, 1404–1417 (2016). https://doi.org/10.1007/s12272-016-0732-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12272-016-0732-x

Keywords

Navigation