A novel lipid nanoemulsion system for improved permeation of granisetron

被引:27
作者
Doh, Hea-Jeong [1 ]
Jung, Yunjin [1 ]
Balakrishnan, Prabagar [2 ,3 ]
Cho, Hyun-Jong [4 ]
Kim, Dae-Duk [2 ,3 ]
机构
[1] Pusan Natl Univ, Coll Pharm, Pusan 609735, South Korea
[2] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[3] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[4] Sunchon Natl Univ, Coll Pharm, Sunchon 540950, South Korea
基金
新加坡国家研究基金会;
关键词
Anti-emetics; Caco-2; cell; Enhanced permeation; Granisetron; Lipid nanoemulsion; DRUG-DELIVERY SYSTEMS; IN-VIVO EVALUATION; ORAL BIOAVAILABILITY; INTRANASAL DELIVERY; ENHANCED SOLUBILITY; FORMULATION; ABSORPTION; TRANSPORT; VITRO; DISSOLUTION;
D O I
10.1016/j.colsurfb.2012.07.019
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new lipid nanoemulsion (DIE) system containing granisetron (GRN) was developed and its in vitro permeation-enhancing effect was evaluated using Caco-2 cell monolayers. Particle size, polydispersity index (PI) and stability of the prepared GRN-loaded LNE systems were also characterized. The mean diameters of prepared LNEs were around 50 nm with PI < 0.2. Developed LNEs were stable at 4 degrees C in the dark place over a period of 12 weeks. In vitro drug dissolution and cytotoxicity studies of GRN-loaded LNEs were performed. GRN-loaded LNEs exhibited significantly higher drug dissolution than GRN suspension at pH 6.8 for 2h (P<0.05). In vitro permeation study in Caco-2 cell monolayers showed that the LNEs significantly enhanced the drug permeation compared to GRN powder. The in vivo toxicity study in the rat jejunum revealed that the prepared GRN-loaded LNE was as safe as the commercial formulation (Kytril). These results suggest that LNE could be used as a potential oral liquid formulation of GRN for anti-emetic treatment on the post-operative and chemotherapeutic patients. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:475 / 480
页数:6
相关论文
共 31 条
[1]   5-HT3-receptor antagonists in the management of nausea and vomiting in cancer and cancer treatment [J].
Aapro, M .
ONCOLOGY, 2005, 69 (02) :97-109
[2]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[3]  
Ammar H. O., 2006, Current Drug Delivery, V3, P333, DOI 10.2174/156720106777731037
[4]  
Babu RJ, 2008, DRUG DELIV, V15, P381, DOI [10.1080/10717540802006922, 10.1080/10717540802006922 ]
[5]   Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS) [J].
Balakrishnan, Prabagar ;
Lee, Beom-Jin ;
Oh, Dong Hoon ;
Kim, Jong Oh ;
Hong, Myung Ja ;
Jee, Jun-Pil ;
Kim, Jung Ae ;
Yoo, Bong Kyu ;
Woo, Jong Soo ;
Yong, Chul Soon ;
Choi, Han-Gon .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 72 (03) :539-545
[6]   Enhanced oral bioavailability of Coenzyme Q10 by self-emulsifying drug delivery systems [J].
Balakrishnan, Prabagar ;
Lee, Beom-Jin ;
Oh, Dong Hoon ;
Kim, Jong Oh ;
Lee, Young-Im ;
Kim, Dae-Duk ;
Jee, Jun-Pil ;
Lee, Yong-Bok ;
Woo, Jong Soo ;
Yong, Chul Soon ;
Choi, Han-Gon .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 374 (1-2) :66-72
[7]   Study of surfactant combinations and development of a novel nanoemulsion for minimising variations in bioavailability of ezetimibe [J].
Bali, Vikas ;
Ali, Mushir ;
Ali, Javed .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 76 (02) :410-420
[8]   Characterization and in vitro evaluation of freeze-dried microparticles composed of granisetron-cyclodextrin complex and carboxymethylcellulose for intranasal delivery [J].
Cho, Hyun-Jong ;
Balakrishnan, Prabagar ;
Shim, Won-Sik ;
Chung, Suk-Jae ;
Shim, Chang-Koo ;
Kim, Dae-Duk .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 400 (1-2) :59-65
[9]   A comparison of intestinal lymphatic transport and systemic bioavailability of saquinavir from three lipid-based formulations in the anaesthetised rat model [J].
Griffin, Brendan T. ;
O'Driscoll, Caitriona M. .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2006, 58 (07) :917-925
[10]   Comparative effects of different cosurfactants on sterile prednisolone acetate ocular submicron emulsions stability and release [J].
Ibrahim, Shaimaa S. ;
Awad, Gehanne A. S. ;
Geneidi, Ahmed ;
Mortada, Nahed D. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2009, 69 (02) :225-231