Floating capsules containing alginate-based beads of salbutamol sulfate: In vitro-in vivo evaluations

被引:25
作者
Malakar, Jadupati [1 ]
Datta, Prabir Kumar [1 ]
Das Purakayastha, Saikat [1 ]
Dey, Sanjay [1 ]
Nayak, Amit Kumar [2 ]
机构
[1] Bengal Coll Pharmaceut Sci & Res, Dept Pharmaceut, Durgapur 713212, W Bengal, India
[2] Seemanta Inst Pharmaceut Sci, Dept Pharmaceut, Mayurbhanj 757086, Odisha, India
关键词
Salbutamol sulfate; Gastroretention; Floating system; DRUG-DELIVERY SYSTEM; MUCOADHESIVE BEADS; DESIGN; OPTIMIZATION; FORMULATION; RELEASE; TABLET;
D O I
10.1016/j.ijbiomac.2013.11.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The present study deals with the development and evaluations of stomach-specific floating capsules containing salbutamol sulfate-loaded oil-entrapped alginate-based beads. Salbutamol sulfate-loaded oil-entrapped beads were prepared and capsulated within hard gelatin capsules (size 1). The effects of HPMC K4M and potato starch weight masses on drug encapsulation efficiency (DEE) of beads and cumulative drug release at 10 h (R-10h) from capsules was analyzed by 3(2) factorial design. The optimization results indicate increasing of DEE in the oil-entrapped beads and decreasing R-10h from capsules with increment of HPMC K4M and potato starch weight masses. The optimized formulation showed DEE of 70.02 +/- 3.16% and R-10h of 56.96 +/- 2.92%. These capsules showed floatation over 6 h and sustained drug release over 10 h in gastric pH (1.2). In vivo X-ray imaging study of optimized floating capsules in rabbits showed stomach-specific gastroretention over a prolonged period. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 189
页数:9
相关论文
共 38 条
[1]
Drug release kinetics and physicochemical characteristics of floating drug delivery systems [J].
Adibkia, Khosro ;
Hamedeyazdan, Sanaz ;
Javadzadeh, Yousef .
EXPERT OPINION ON DRUG DELIVERY, 2011, 8 (07) :891-903
[2]
Amit kumarNayak., 2010, Journal of pharma education and research, V1, P1
[3]
Design and in vitro evaluation of multiparticulate floating drug delivery system of zolpidem tartarate [J].
Amrutkar, P. P. ;
Chaudhari, P. D. ;
Patil, S. B. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2012, 89 :182-187
[4]
[Anonymous], J PHARM
[5]
[Anonymous], 2000, US PHARM NAT FORM US
[6]
Floating drug delivery systems: A review [J].
Arora, S ;
Ali, J ;
Ahuja, A ;
Khar, RK ;
Baboota, S .
AAPS PHARMSCITECH, 2005, 6 (03) :E372-E390
[7]
Design and release characteristics of sustained release tablet containing metformin HCl [J].
Basak, Subal Chandra ;
Kumar, Kesevan Senthil ;
Ramalingam, Murugesan .
REVISTA BRASILEIRA DE CIENCIAS FARMACEUTICAS, 2008, 44 (03) :477-483
[8]
Floating bioadhesive drug delivery system using novel effervescent agents [J].
Belgamwar, V. S. ;
Surana, S. J. .
ASIAN JOURNAL OF PHARMACEUTICS, 2009, 3 (02) :156-160
[9]
Design and Development of Oral Mucoadhesive Multiparticulate System Containing Atenolol: in Vitro-in Vivo Characterization [J].
Belgamwar, Veena Shailendra ;
Surana, Sanjay Javerilal .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2010, 58 (09) :1168-1175
[10]
Ionotropically emulsion gelled polysaccharides beads: Preparation, in vitro and in vivo evaluation [J].
Elmowafy, Enas M. ;
Awad, Gehanne A. S. ;
Mansour, Samar ;
El-Shamy, Abd El-Hamid A. .
CARBOHYDRATE POLYMERS, 2009, 75 (01) :135-142