Solvent-Cast Polymeric Films from Pectin and Eudragit(R) NE 30D for Transdermal Drug Delivery Systems

被引:12
作者
Suksaeree, Jirapornchai [1 ]
Maneewattanapinyo, Pattwat [1 ]
Panrat, Kamon [2 ]
Pichayakorn, Wiwat [3 ]
Monton, Chaowalit [4 ]
机构
[1] Rangsit Univ, Coll Pharm, Dept Pharmaceut Chem, Muang 12000, Pathum Thani, Thailand
[2] Prince Songkla Univ, Fac Pharmaceut Sci, Pharmaceut Lab Serv Ctr, Hat Yai 90112, Songkhla, Thailand
[3] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Hat Yai 90112, Songkhla, Thailand
[4] Rangsit Univ, Coll Pharm, Drug & Herbal Prod Res & Dev Ctr, Muang 12000, Pathum Thani, Thailand
关键词
Pectin; Eudragit(&#174); NE; 30D; Ionic liquid drug; Solvent‐ cast polymeric films; Transdermal drug delivery systems; IN-VITRO EVALUATION; IONIC LIQUIDS; CONTROLLED-RELEASE; BUCCAL FILMS; LIDOCAINE; PATCHES; MATRIX; ETHYLCELLULOSE; PERMEATION; DESIGN;
D O I
10.1007/s10924-021-02108-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, solvent-cast polymeric films containing ionic liquid lidocaine/aspirin for transdermal patches were developed. Solvent-cast polymeric films were prepared from two polymers, pectin and Eudragit(R) NE 30D, by drying the polymeric solution in a hot air oven at 70 +/- 3 degrees C for 10 h. Glycerin was used as a plasticizer. Lidocaine and aspirin were prepared in ionic liquid form and loaded into the patches. The physicomechanical properties of the films were characterized by texture analysis, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction. A scanning electron microscope was used to photograph the surfaces of solvent-cast polymeric films. Eudragit(R) NE 30D significantly decreased the toughness and rigidity of the films. The transdermal patches were in the amorphous state, and their thermal properties were not changed from blank polymeric films. The surfaces of transdermal patches were rougher than blank polymeric films and revealed the distribution of the drug. Eudragit(R) NE 30D significantly decreased the trends of entrapment efficiency and in vitro release of lidocaine and aspirin drugs. The kinetic release observed in vitro fitted to Higuchi's model rather than zero and first order models, indicating that a diffusion mechanism governed the release of the drug from the patch. Thus, the solvent-cast polymeric films from two polymers, pectin and Eudragit(R) NE 30D, are suitable for transdermal patches loaded with ionic liquid lidocaine/aspirin.
引用
收藏
页码:3174 / 3184
页数:11
相关论文
共 38 条
[1]   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
[2]   Transdermal Bioavailability in Rats of Lidocaine in the Forms of Ionic Liquids, Salts, and Deep Eutectic [J].
Berton, Paula ;
Di Bona, Kristin R. ;
Yancey, Denise ;
Rizvi, Syed A. A. ;
Gray, Marquita ;
Gurau, Gabriela ;
Shamshina, Julia L. ;
Rasco, Jane F. ;
Rogers, Robin D. .
ACS MEDICINAL CHEMISTRY LETTERS, 2017, 8 (05) :498-503
[3]   In search of pure liquid salt forms of aspirin: ionic liquid approaches with acetylsalicylic acid and salicylic acid [J].
Bica, Katharina ;
Rijksen, Christiaan ;
Nieuwenhuyzen, Mark ;
Rogers, Robin D. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (08) :2011-2017
[4]   Development and mechanical characterization of solvent-cast polymeric films as potential drug delivery systems to mucosal surfaces [J].
Boateng, Joshua S. ;
Stevens, Howard N. E. ;
Eccleston, Gillian M. ;
Auffret, Anthony D. ;
Humphrey, Michael J. ;
Matthews, Kerr H. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2009, 35 (08) :986-996
[5]   A novel polymethylmethacrylate hydrophilic adhesive matrix intended for transdermal patch formulations [J].
Cilurzo, Francesco ;
Minghetti, Paola ;
Gennari, Chiara G. M. ;
Casiraghi, Antonella ;
Montanari, Luisa .
DRUG DELIVERY, 2010, 17 (03) :171-177
[6]   Development and In Vitro-In Vivo Evaluation of Fenretinide-Loaded Oral Mucoadhesive Patches for Site-Specific Chemoprevention of Oral Cancer [J].
Desai, Kashappa-Goud H. ;
Mallery, Susan R. ;
Holpuch, Andrew S. ;
Schwendeman, Steven P. .
PHARMACEUTICAL RESEARCH, 2011, 28 (10) :2599-2609
[7]   Ionic liquids as ingredients in topical drug delivery systems [J].
Dobler, Dorota ;
Schmidts, Thomas ;
Klingenhoefer, Ines ;
Runkel, Frank .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 441 (1-2) :620-627
[8]   Development and in vitro evaluation of diltiazem hydrochloride transdermal patches based on povidone-ethylcellulose matrices [J].
Gupta, R ;
Mukherjee, B .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (01) :1-7
[9]   Effect of polydimethylsiloxane and ethylcellulose on in vitro permeation of centchroman from its transdermal patches [J].
Gupta, Varsha ;
Singh, Swati ;
Srivarstava, Madhumita ;
Ahmad, Hafsa ;
Pachauri, Shakti Deep ;
Khandelwal, Kiran ;
Dwivedi, Pankaj ;
Dwivedi, Anil Kumar .
DRUG DELIVERY, 2016, 23 (01) :113-122
[10]   The third evolution of ionic liquids:: active pharmaceutical ingredients [J].
Hough, Whitney L. ;
Smiglak, Marcin ;
Rodriguez, Hector ;
Swatloski, Richard P. ;
Spear, Scott K. ;
Daly, Daniel T. ;
Pernak, Juliusz ;
Grisel, Judith E. ;
Carliss, Richard D. ;
Soutullo, Morgan D. ;
Davis, James H., Jr. ;
Rogers, Robin D. .
NEW JOURNAL OF CHEMISTRY, 2007, 31 (08) :1429-1436