Preparation and evaluation of solid lipid nanoparticles based nanogel for dermal delivery of meloxicam

被引:99
作者
Khurana, S. [1 ]
Bedi, P. M. S. [1 ]
Jain, N. K. [2 ]
机构
[1] Guru Nanak Dev Univ, Dept Pharmaceut Sci, Amritsar 143104, Punjab, India
[2] Dr Hari Singh Gour Vishwavidyalaya, Dept Pharmaceut Sci, Sagar 470003, India
关键词
Solid lipid nanoparticles; Meloxicam; Skin penetration; Controlled release; Sustained release; Carrageenan induced paw edema model; GASTROINTESTINAL DISORDERS; TRANSDERMAL DELIVERY; TOPICAL DELIVERY; DRUG-DELIVERY; GEL; SPECTROSCOPY; DICLOFENAC; PARAMETERS; CERAMIDES; RELEASE;
D O I
10.1016/j.chemphyslip.2013.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the current investigation was to prepare and investigate the potential of solid lipid nanoparticles based gel (SLN-gel) for the dermal delivery of meloxicam (MLX). The meloxicam loaded SLN (MLX-SLN) gel was developed and characterized by means of photon correlation spectroscopy, rheometry, and differential scanning calorimetry to determine the physicochemical properties. The behavior of SLN gel on rat skin was evaluated in vitro using Franz diffusion cells to determine the skin permeation and penetration characteristics, in vivo on mice to determine the skin tolerance by histopathological examinations. The anti-inflammatory potential of SLN gel was assessed by carrageenan induced rat paw edema test. Biophysical studies including differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR) were undertaken to study the interaction between the SLN gel and skin. MLX-SLN gel with nanometric particle size exhibited the controlled release abilities and simultaneously the potential to transport the drug to various skin layers. SLN gel displayed viscoelastic properties with predominantly elastic behavior and exhibited plastic flow. Biophysical studies elucidated the interaction between the SLN gel and stratum corneum (SC) lipids, and proposed the lipid bilayer fluidization as the possible mechanism for the increased penetration of meloxicam into skin. The nano-gel system showed marked anti-inflammatory activity and excellent skin tolerability. It can be concluded that SLN gel may be a promising delivery system for MLX in the treatment of inflammatory disorders. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:65 / 72
页数:8
相关论文
共 37 条
[1]   Biologics in development for rheumatoid arthritis: Relevance to osteoarthritis [J].
Abramson, Steven B. ;
Yazici, Yusuf .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (02) :212-225
[2]   Penetration of drugs through skin, a complex rate-controlling membrane [J].
Bolzinger, Marie-Alexandrine ;
Briancon, Stephanie ;
Pelletier, Jocelyne ;
Chevalier, Yves .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2012, 17 (03) :156-165
[3]   Preparation and characterization of lipid based nanosystems for topical delivery of quercetin [J].
Bose, Sonali ;
Michniak-Kohn, Bozena .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 48 (03) :442-452
[4]   Rheology of polymer blends: linear model for viscoelastic emulsions [J].
Bousmina, M .
RHEOLOGICA ACTA, 1999, 38 (01) :73-83
[5]   Rheological studies on solid lipid nanoparticle based carbopol gels of aceclofenac [J].
Chawla, Viney ;
Saraf, Shubhini A. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2012, 92 :293-298
[6]   Penetratin-induced transdermal delivery from HII mesophases of sodium diclofenac [J].
Cohen-Avrahami, Marganit ;
Libster, Dima ;
Aserin, Abraham ;
Garti, Nissim .
JOURNAL OF CONTROLLED RELEASE, 2012, 159 (03) :419-428
[7]   Preparation and characteristics of oridonin-loaded nanostructured lipid carriers as a controlled-release delivery system [J].
Dai, Wenting ;
Zhang, Dianrui ;
Duan, Cunxian ;
Jia, Lejiao ;
Wang, Yancai ;
Feng, Feifei ;
Zhang, Qiang .
JOURNAL OF MICROENCAPSULATION, 2010, 27 (03) :234-241
[8]   Solid lipid nanoparticles and nanoemulsions containing ceramides: Preparation and physicochemical characterization [J].
Deli, Georgia ;
Hatziantoniou, Sophia ;
Nikas, Yorgos ;
Demetzos, Costas .
JOURNAL OF LIPOSOME RESEARCH, 2009, 19 (03) :180-188
[9]   PREPARATION AND STRUCTURE OF A WATER-IN-OIL CREAM CONTAINING LIPID NANOPARTICLES [J].
DEVRINGER, T ;
DERONDE, HAG .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (04) :466-472
[10]  
Distel M, 1996, BRIT J RHEUMATOL, V35, P68