Bacopasaponin C: Critical evaluation of anti-leishmanial properties in various delivery modes

被引:32
作者
Sinha, J [1 ]
Raay, B [1 ]
Das, N [1 ]
Medda, S [1 ]
Garai, S [1 ]
Mahato, SB [1 ]
Basu, MK [1 ]
机构
[1] Indian Inst Chem Biol, Biomembrane Div, Kolkata 700032, W Bengal, India
关键词
Bacapasaponin C; Efficacy versus Size; liposomes; microspheres; nanocapsules; niosomes;
D O I
10.1080/107175402753413181
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bacopasaponin C, an indigenous glycoside, was isolated from Indian medicinal plant Bacopa monniera (b. brahmi) and was tested for antileishmanial properties both in free and in various delivery modes, e. g., niosomes, microspheres, and nanoparticles that are used now as alternatives to more commonly used liposomes. The different vesicles were prepared by published protocols. The percent intercalation of Bacopasaponin C in liposomes, niosomes, and micropspheres determined at its absorption maximal (lambdamax = 238 nm, epsilon= 8.6 x 10(3) M-1 cm(-1)) was found to be 30; for nanoparticles it was 50. At equivalent dose of 1.75 mg/kg body weight, every third day for a total of 6 doses in 15 days, Bacopasaponin C in all the vesicular forms was found to be very active. An inverse linear relationship between the efficacy and the size of the vesicles was established. As analyzed from tissue histology, blood pathology, and specific tests related to normal liver and kidney functions, Bacopasaponin C in each of the four vesicular forms was found to be without any side effects. Thus, because of its indigenous origin and non-toxic nature, Bacopasaponin C could very well be considered for application in the clinic through these alternative delivery modes.
引用
收藏
页码:55 / 62
页数:8
相关论文
共 28 条
[1]  
ALLEMANN E, 1993, EUR J PHARM BIOPHARM, V39, P173
[2]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[3]   THE PREPARATION AND PROPERTIES OF NIOSOMES NON-IONIC SURFACTANT VESICLES [J].
BAILLIE, AJ ;
FLORENCE, AT ;
HUME, LR ;
MUIRHEAD, GT ;
ROGERSON, A .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1985, 37 (12) :863-868
[4]  
DATTA AK, 1987, J BIOL CHEM, V262, P5515
[5]   POLYMERIC MICROSPHERES AS DRUG CARRIERS [J].
DAVIS, SS ;
ILLUM, L .
BIOMATERIALS, 1988, 9 (01) :111-115
[6]   MICROSPHERES FOR TARGETING DRUGS TO SPECIFIC BODY SITES [J].
DAVIS, SS ;
ILLUM, L ;
MOGHIMI, SM ;
DAVIES, MC ;
PORTER, CJH ;
MUIR, IS ;
BRINDLEY, A ;
CHRISTY, NM ;
NORMAN, ME ;
WILLIAMS, P ;
DUNN, SE .
JOURNAL OF CONTROLLED RELEASE, 1993, 24 (1-3) :157-163
[7]   Antileishmanial activity of three saponins isolated from ivy, α-hederin, β-hederin and hederacolchiside A1, as compared to their action on mammalian cells cultured in vitro [J].
Delmas, F ;
Di Giorgio, C ;
Elias, R ;
Gasquet, M ;
Azas, N ;
Mshvildadze, V ;
Dekanosidze, G ;
Kemertelidze, E ;
Timon-David, P .
PLANTA MEDICA, 2000, 66 (04) :343-347
[8]   Dammarane-type triterpenoid saponins from Bacopa monniera [J].
Garai, S ;
Mahato, SB ;
Ohtani, K ;
Yamasaki, K .
PHYTOCHEMISTRY, 1996, 42 (03) :815-820
[9]   THE CONTROLLED INTRAVENOUS DELIVERY OF DRUGS USING PEG-COATED STERICALLY STABILIZED NANOSPHERES [J].
GREF, R ;
DOMB, A ;
QUELLEC, P ;
BLUNK, T ;
MULLER, RH ;
VERBAVATZ, JM ;
LANGER, R .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :215-233
[10]   LYSOSOMAL LOCALIZATION OF BETA-FRUCTOFURANOSIDASE-CONTAINING LIPOSOMES INJECTED INTO RATS - SOME IMPLICATIONS IN TREATMENT OF GENETIC DISORDERS [J].
GREGORIADIS, G ;
RYMAN, BE .
BIOCHEMICAL JOURNAL, 1972, 129 (01) :123-+