Development and evaluation of anti-malarial bio-conjugates: artesunate-loaded nanoerythrosomes

被引:0
作者
Jaya Agnihotri
Shubhini Saraf
Sobhna Singh
Papiya Bigoniya
机构
[1] H. K College of Pharmacy,School of Biosciences & Biotechnology
[2] Babasaheb Bhimrao Ambedkar University,School of Pharmaceutical Sciences
[3] MJP Rohilkhand University,undefined
[4] Radharaman College of Pharmacy,undefined
来源
Drug Delivery and Translational Research | 2015年 / 5卷
关键词
Anti-malarial; Artesunate; Cellular carrier; Erythrocytes; Nanoerythrocytes; Targeting;
D O I
暂无
中图分类号
学科分类号
摘要
Biodegradable cellular carrier has desired properties for achieving effective long-term controlled release of drugs having short half life. To reduce the undesired effects of drug, advanced drug delivery systems are needed which are based on specific cell targeting module. Artesunate (ART) conjugation on nanoerythrosomes (NE) can have controlled delivery to avoid drug leakage, increase the stability, and reduce cost and toxicities. In this study nanosized lipoprotein membrane vesicles bearing ART were prepared by extrusion method. Developed ART-NE conjugate formulations were optimized on the basis of vesicle morphology, size and size distribution, polydispersity index, integrity of membrane, loaded drug concentration, drug leakage, effect of temperature and viscosity, syringeability, in vitro release profile and in vivo plasma concentration estimation studies. Fourier transform infrared (FTIR) spectroscopy reveals that lipid chain order of RBCs are insignificantly affected in moderate conditions after ART loading. The formulated ART-NE carrier revealed non aggregated, uniformly sized particles with smooth surfaces. The maximum drug loading was found to be 25.20 ± 1.3 μg/ml. ART-NE formulation was best fit for zero order kinetics and was found to be capable of controlled release of drug for 8 hrs. ART-NE formulation showed good redispersibility with desirable properties for parenteral administration. Formulation was stable when subjected to stress by centrifugal force of 7500 rpm and could bear turbulence shock of 15 passes from hypodermic needle of size 23 gauges. The ART-NE formulation administered intravenously showed higher plasma concentration compared to free drug signifying not only controlled release but higher rate of in vivo release. The developed formulation exhibited zero order release profile as per kinetic study analysis suggesting the suitability of carrier for the sustained and targeted delivery of ART. The developed ART-NE drug delivery system offers improved pharmacokinetic profile with assurance of increased therapeutic efficacy.
引用
收藏
页码:489 / 497
页数:8
相关论文
共 74 条
  • [1] Anvikar AR(2014)Anti malarial drug policy in India: Past, present and future Ind J Med Res 139 205-15
  • [2] Arora U(2010)Firstborn microcrystallization method to prepare nanocapsules containing Artesunate Int J Nanomedicine 5 483-6
  • [3] Sonal GS(1997)Assessment of the pharmacodynamic properties of antimalarial drugs in vivo Antimicrob Agents Chemother 41 1413-22
  • [4] Mishra N(1991)The dynamics of drug resistance in Pharmacol Ther 50 95-121
  • [5] Shahi B(1994)Artemisinin: current status Trans R Soc Trop Med Hyg 88 S3-4
  • [6] Savargaonkar D(2014)Nanocapsules based on mPEGylated artesunate prodrug and its cytotoxicity Colloid Surf B 115 164-9
  • [7] Xiao XC(2013)Formal chemical stability analysis and solubility analysis of artesunate and hydroxychloroquinine for development of parenteral dosage form J Pharm Res 6 117-22
  • [8] Hon Z(2012)Artesunate-loaded chitosan/lecithin nanoparticles: preparation, characterization, and in vivo studies Drug Dev Ind Pharm 38 1538-46
  • [9] White NJ(2015)Enhancing the in vitro anti-cancer efficacy of artesunate by loading into polyd, l-lactide-co-glycolide (PLGA) nanoparticles Arch Pharm Res 38 716-24
  • [10] Wernsdorfer WH(1996)Chemical stability of artesunate injection and proposal for its administration by intravenous infusion J Pharm Pharmacol 48 22-6