Generation and precipitation of paclitaxel nanoparticles in basil seed mucilage via combination of supercritical gas antisolvent and phase inversion techniques

被引:26
作者
Akbari, I. [1 ]
Ghoreishi, S. M. [1 ]
Habibi, N. [2 ]
机构
[1] Isfahan Univ Technol, Dept Chem Engn, Esfahan 8415683111, Iran
[2] Isfahan Univ Technol, Nanotechnol & Adv Mat Inst, Esfahan 8415683111, Iran
关键词
Natural polymer; Basil seed mucilage; Supercritical fluid; Paclitaxel; Nano particle; Drug loading; DRUG-DELIVERY; IN-VITRO; CARBON-DIOXIDE; GUAR GUM; POLYSACCHARIDE; MICROPARTICLES; FORMULATION; POLYMERS; KINETICS; BEHAVIOR;
D O I
10.1016/j.supflu.2014.07.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In recent years, plant derived polymers have evoked tremendous interest in the field of drug delivery. In this work, a promising anticancer drug, paclitaxel, was precipitated in the basil seeds mucilage (BSM) using supercritical carbon dioxide (SC-CO2). The employed SC-CO2 process in this research is a combination of gas antisolvent and phase inversion techniques and consists of two steps: (1) casting solution preparation, a uniform mixture of BSM, water, paclitaxel and dimethyl sulfoxide (DMSO), (2) simultaneous generation and precipitation of nanoparticles in BSM structure using SC-CO2 as antisolvent. The effect of DMSO/water ratio (4 and 6 (v/v)), pressure (10-16 MPa) and CO2 addition rate (1-3 mL/min) on mean particle size (MPS), particle size distribution (PSD) and drug loading efficiency (DLE) were studied. Particle analyses were performed by scanning electron microscopy (SEM) and Zetasizer. High performance liquid chromatography was utilized for studying DLE. Nanoparticles of paclitaxel (MPS of 117-200 nm depending on process variables) with narrow PSD were successfully precipitated in BSM structure with DLE of 56.8-78.2%. The FTIR spectra confirmed that paclitaxel actually precipitated in basil seeds mucilage. Experimental results indicated that higher DMSO/water ratio, pressure and CO2 addition decreased MPS and DLE. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 188
页数:7
相关论文
共 45 条
[1]   Phase equilibria of dimethyl sulfoxide (DMSO) plus carbon dioxide, and DMSO plus carbon dioxide plus water mixtures [J].
Andreatta, A. E. ;
Florusse, L. J. ;
Bottini, S. B. ;
Peters, C. J. .
JOURNAL OF SUPERCRITICAL FLUIDS, 2007, 42 (01) :60-68
[2]   Preparation and characterization of mucilage polysaccharide for biomedical applications [J].
Archana, G. ;
Sabina, K. ;
Babuskin, S. ;
Radhakrishnan, K. ;
Fayidh, Mohammed A. ;
Babu, P. Azhagu Saravana ;
Sivarajan, M. ;
Sukumar, M. .
CARBOHYDRATE POLYMERS, 2013, 98 (01) :89-94
[3]  
Avachat AM, 2011, INDIAN J PHARM EDUC, V45, P86
[4]   Experimental study of the GAS process for producing microparticles of beclomethasone-17,21-dipropionate suitable for pulmonary delivery [J].
Bakhbakhi, Y ;
Charpentier, PA ;
Rohani, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 309 (1-2) :71-80
[5]   Generation of chitosan nanoporous structures for tissue engineering applications using a supercritical fluid assisted process [J].
Cardea, S. ;
Pisanti, P. ;
Reverchon, E. .
JOURNAL OF SUPERCRITICAL FLUIDS, 2010, 54 (03) :290-295
[6]   Plasticizer concentration and the performance of a diffusion-controlled polymeric drug delivery system [J].
Chamarthy, Sai Prasanth ;
Pinal, Rodolfo .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 331 (1-2) :25-30
[7]   Protein nanoparticles formation by supercritical antisolvent with enhanced mass transfer [J].
Chattopadhyay, P ;
Gupta, RB .
AICHE JOURNAL, 2002, 48 (02) :235-244
[8]   Gas antisolvent precipitation of Ginkgo ginkgolides with supercritical CO2 [J].
Chen, KX ;
Zhang, XY ;
Pan, J ;
Zhang, WC ;
Yin, WH .
POWDER TECHNOLOGY, 2005, 152 (1-3) :127-132
[9]   Natural polymers for gene delivery and tissue engineering [J].
Dang, Jiyoung M. ;
Leong, Kam W. .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (04) :487-499
[10]   Paclitaxel-loaded PEGylated PLGA-based nanoparticles: In vitro and in vivo evaluation [J].
Danhier, Fabienne ;
Lecouturier, Nathalie ;
Vroman, Benoit ;
Jerome, Christine ;
Marchand-Brynaert, Jacqueline ;
Feron, Olivier ;
Preat, Veronique .
JOURNAL OF CONTROLLED RELEASE, 2009, 133 (01) :11-17