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

被引:10
|
作者
Agnihotri, Jaya [1 ]
Saraf, Shubhini [2 ]
Singh, Sobhna [3 ]
Bigoniya, Papiya [4 ]
机构
[1] HK Coll Pharm, Bombay, Maharashtra, India
[2] Babasaheb Bhimrao Ambedkar Univ, Sch Biosci & Biotechnol, Lucknow, Uttar Pradesh, India
[3] MJP Rohilkhand Univ, Sch Pharmaceut Sci, Bareilly, Uttar Pradesh, India
[4] Radharaman Coll Pharm, Bhopal, MP, India
关键词
Anti-malarial; Artesunate; Cellular carrier; Erythrocytes; Nanoerythrocytes; Targeting; CELLULAR CARRIER; DRUG; DELIVERY; NANOCAPSULES;
D O I
10.1007/s13346-015-0246-y
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
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 mu g/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:9
相关论文
共 50 条
  • [1] Development and evaluation of anti-malarial bio-conjugates: artesunate-loaded nanoerythrosomes
    Jaya Agnihotri
    Shubhini Saraf
    Sobhna Singh
    Papiya Bigoniya
    Drug Delivery and Translational Research, 2015, 5 : 489 - 497
  • [2] The anti-malarial artesunate is also active against cancer
    Efferth, T
    Dunstan, H
    Sauerbrey, A
    Miyachi, H
    Chitambar, CR
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2001, 18 (04) : 767 - 773
  • [3] Engineered cellular carrier nanoerythrosomes as potential targeting vectors for anti-malarial drug
    Agnihotri, Jaya
    Gajbhiye, Virendra
    Jain, Narendra Kumar
    ASIAN JOURNAL OF PHARMACEUTICS, 2010, 4 (02) : 116 - 120
  • [4] Inhibition of tumor angiogenesis in vitro and in vivo by the anti-malarial artesunate
    Efferth, T
    Dell'Eva, R
    Vené, R
    Anfosso, L
    Forlani, A
    Albini, A
    Pfeffe, U
    EUROPEAN JOURNAL OF CELL BIOLOGY, 2005, 84 : 94 - 94
  • [5] Anti-malarial efficacy of pyronaridine and artesunate in combination in vitro and in vivo
    Vivas, Livia
    Rattray, Lauren
    Stewart, Lindsay
    Bongard, Emily
    Robinson, Brian L.
    Peters, Wallace
    Croft, Simon L.
    ACTA TROPICA, 2008, 105 (03) : 222 - 228
  • [6] Development of electrosprayed artesunate-loaded core-shell nanoparticles
    Hoang Nhan Ho
    Laidmae, Ivo
    Kogermann, Karin
    Lust, Andres
    Meos, Andres
    Chien Ngoc Nguyen
    Heinamaki, Jyrki
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2017, 43 (07) : 1134 - 1142
  • [7] Formulation development and evaluation of the anti-malaria properties of sustained release artesunate-loaded solid lipid microparticles based on phytolipids
    Chinaeke, E. E.
    Chime, S. A.
    Onyishi, V. I.
    Attama, A. A.
    Okore, V. C.
    DRUG DELIVERY, 2015, 22 (05) : 652 - 665
  • [8] Artesunate, an anti-malarial drug, has a potential to inhibit HCV replication
    Rongjuan Dai
    Xinqiang Xiao
    Feng Peng
    Mingming Li
    Guozhong Gong
    Virus Genes, 2016, 52 : 22 - 28
  • [9] Artesunate, an anti-malarial drug, has a potential to inhibit HCV replication
    Dai, Rongjuan
    Xiao, Xinqiang
    Peng, Feng
    Li, Mingming
    Gong, Guozhong
    VIRUS GENES, 2016, 52 (01) : 22 - 28
  • [10] DEVELOPMENT OF MEFLOQUINE AS AN ANTI-MALARIAL DRUG
    不详
    BULLETIN OF THE WORLD HEALTH ORGANIZATION, 1983, 61 (02): : 169 - 178