Use of Isolated Pectin from a Cissampelos pareira-Based Polymer Blend Matrix for the Transdermal Delivery of Nicotine

被引:15
作者
Suksaeree, Jirapornchai [1 ]
Karnsopa, Phatipan [1 ]
Wannaphruek, Nannapat [1 ]
Prasomkij, Jessada [1 ]
Panrat, Kamon [2 ]
Monton, Chaowalit [3 ]
Pichayakorn, Wiwat [4 ]
机构
[1] Rangsit Univ, Fac Pharm, Dept Pharmaceut Chem, Pathum Thani 12000, Thailand
[2] Prince Songkla Univ, Fac Pharmaceut Sci, Pharmaceut Lab Serv Ctr, Hat Yai 90112, Songkhla, Thailand
[3] Rangsit Univ, Fac Pharm, Herbal Med Prod Res & Dev Ctr, Muang 12000, Pathum Thani, Thailand
[4] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Hat Yai 90112, Songkhla, Thailand
关键词
Cissampelos pareira leaves; Krueo Ma Noy; Deproteinized natural rubber latex; Nicotine transdermal patches; Pectin; NATURAL-RUBBER LATEX; DRUG-DELIVERY; FILMS;
D O I
10.1007/s10924-018-1233-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pectin is a natural biopolymer, and a major component of a complex heterogeneous polysaccharide found in the primary cell walls and middle lamella of plant tissues. This paper used pectin isolated from Cissampelos pareira (Krueo Ma Noy) leaves to prepare the matrix layer for nicotine transdermal patches. However, the patch was a brittle film, thus, deproteinized natural rubber latex (DNRL) was blended to improve flexibility of the patch. Here we present for the first time a preparation study exploring the suitability of isolated pectin blends to serve as drug carriers and the mechanism controlling the release patterns of nicotine. The hydrophilicity of the patches was found to decrease when increasing the DNRL ratio. Differential scanning calorimetry and X-ray diffraction experiments were used to characterize the interactions between the investigated drugs and the matrix polymers. In vitro studies showed that the isolated pectin blends were an effective matrix for controlled nicotine release. The release and permeation patterns of nicotine depend on the hydrophilicity of the patches. The kinetic models of nicotine were found to be a Higuchi model and zero order for in vitro release and skin permeation, respectively.
引用
收藏
页码:3531 / 3539
页数:9
相关论文
共 38 条
[1]   Nicotine and cotinine modulate cerebral microvascular permeability and protein expression of ZO-1 through nicotinic acetylcholine receptors expressed on brain endothelial cells [J].
Abbruscato, TJ ;
Lopez, SP ;
Mark, KS ;
Hawkins, BT ;
Davis, TP .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (12) :2525-2538
[2]   Formulation and In Vitro Evaluation of Xanthan Gum or Carbopol 934-Based Mucoadhesive Patches, Loaded with Nicotine [J].
Abu-Huwaij, Rana ;
Obaidat, Rana M. ;
Sweidan, Kamal ;
Al-Hiari, Yusuf .
AAPS PHARMSCITECH, 2011, 12 (01) :21-27
[3]   Design and Evaluation of Polysaccharide-Based Transdermal Films for the Controlled Delivery of Nifedipine [J].
Bektas, Aysegul ;
Cevher, Erdal ;
Gungor, Sevgi ;
Ozsoy, Yildiz .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2014, 62 (02) :144-152
[4]   DIURETIC ACTIVITY OF PLANTS USED FOR THE TREATMENT OF URINARY AILMENTS IN GUATEMALA [J].
CACERES, A ;
GIRON, LM ;
MARTINEZ, AM .
JOURNAL OF ETHNOPHARMACOLOGY, 1987, 19 (03) :233-245
[5]  
Cui S, 2006, DETECTION DETERMINAT
[6]   Development of moisture vapour permeable waterproof cotton fabric by coating with blend of natural rubber latex and polyvinyl alcohol [J].
Das, D. ;
Chaudhuri, A. ;
Mitra, M. ;
Ghosh, S. .
JOURNAL OF THE TEXTILE INSTITUTE, 2017, 108 (08) :1285-1290
[7]   Smoking, nicotine and neuropsychiatric disorders [J].
Dome, Peter ;
Lazary, Judit ;
Kalapos, Miklos Peter ;
Rihmer, Zoltan .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2010, 34 (03) :295-342
[8]   Development of Active Films From Pectin and Fruit Extracts: Light Protection, Antioxidant Capacity, and Compounds Stability [J].
Eca, Kaliana S. ;
Machado, Mariana T. C. ;
Hubinger, Miriam D. ;
Menegalli, Florencia C. .
JOURNAL OF FOOD SCIENCE, 2015, 80 (11) :C2389-C2396
[9]   Nicotiana glauca (Tree Tobacco) Intoxication-Two Cases in One Family [J].
Furer V. ;
Hersch M. ;
Silvetzki N. ;
Breuer G.S. ;
Zevin S. .
Journal of Medical Toxicology, 2011, 7 (1) :47-51
[10]  
Gilbert SG, 2004, NICOTINE