Low Protein Natural Rubber Latex - Based Polymer Blends for Transdermal Patches of Mefenamic Acid

Article Preview

Abstract:

Transdermal patches are attraction and acceptance for the patient due to avoid first-pass metabolism, easy to administer and removal, allows rapid termination of treatment if required etc. Low protein natural rubber latex (LPNRL) is a natural polymer that removed the allergic protein from fresh NRL prepared by treatment with proteolytic enzyme and centrifuging process. LPNRL is used for medical skin applications with the non-allergenic product. The objective of this research aimed to prepare the mefenamic acid – loaded transdermal patches made from LPNRL blended with either hydroxypropyl methylcellulose (HPMC) or polyvinyl alcohol (PVA), glycerin and polyvinylpyrrolidone were used as plasticizer and crystallization inhibitor, respectively. The moisture uptake and swelling ratio showed the increment value after either HPMC or PVA was blended in LPNRL because of the increment of their hydrophilicity. These patches showed the homogeneous films that observed by the researcher. The in vitro release showed a faster release rate after either HPMC or PVA was blended in LPNRL. It was concluded that mefenamic acid – loaded transdermal patches could be prepared by using LPNRL blended with either HPMC or PVA as matrix film former could provide an increased and controlled release of the drug. Moreover, it was safe to apply on the skin as did not cause irritation.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

34-38

Citation:

Online since:

August 2020

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2020 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] B.W. Barry, Novel mechanisms and devices to enable successful transdermal drug delivery, Eur J Pharm Sci. 14 (2001) 101-114.

DOI: 10.1016/s0928-0987(01)00167-1

Google Scholar

[2] C. Valenta and B.G. Auner, The use of polymers for dermal and transdermal delivery, Eur J Pharm Biopharm. 58 (2004) 279-289.

Google Scholar

[3] Y.W. Chien, Logics of transdermal controlled drug administration, Drug Dev Ind Pharm. 9 (1983) 497-520.

Google Scholar

[4] G.W. Cleary, Transdermal drug delivery systems. In: A.A. Tracton, (editor). Coatings Materials and Surface Coatings, Florida, CRC Press; 2006, p.64(61-65).

DOI: 10.1201/9781420044058.ch64

Google Scholar

[5] W. Pichayakorn, J. Suksaeree, P. Boonme, W. Taweepreda, and G.C. Ritthidej, Preparation of deproteinized natural rubber latex and properties of films formed by itself and several adhesive polymer blends, Ind Eng Chem Res. 51 (2012) 13393-13404.

DOI: 10.1021/ie301985y

Google Scholar

[6] K. Sanguansap, R. Thonggoom, and P. Tangboriboonrat, Surface modification of natural rubber film by polymerisation of methyl methacrylate in water-based system, Eur Polym J. 42 (2006) 2334-2342.

DOI: 10.1016/j.eurpolymj.2006.06.011

Google Scholar

[7] D. Derouet, P. Intharapat, Q.N. Tran, F. Gohier, and C. Nakason, Graft copolymers of natural rubber and poly(dimethyl(acryloyloxymethyl)phosphonate) (NR-g-PDMAMP) or poly(dimethyl(methacryloyloxyethyl)phosphonate) (NR-g-PDMMEP) from photopolymerization in latex medium, Eur Polym J. 45 (2009) 820-836.

DOI: 10.1016/j.eurpolymj.2008.11.044

Google Scholar

[8] W. Pichayakorn, J. Suksaeree, P. Boonme, T. Amnuaikit, W. Taweepreda, and G.C. Ritthidej, Deproteinized natural rubber latex/hydroxypropylmethyl cellulose blending polymers for nicotine matrix films, Ind Eng Chem Res. 51 (2012) 8442-8452.

DOI: 10.1021/ie300608j

Google Scholar

[9] W. Pichayakorn, J. Suksaeree, P. Boonme, T. Amnuaikit, W. Taweepreda, and G.C. Ritthidej, Nicotine transdermal patches using polymeric natural rubber as the matrix controlling system: Effect of polymer and plasticizer blends, J Membr Sci. 411-412 (2012) 81-90.

DOI: 10.1016/j.memsci.2012.04.017

Google Scholar

[10] J. Suksaeree, L. Charoenchai, C. Monton, T. Chusut, A. Sakunpak, W. Pichayakorn, and P. Boonme, Preparation of a pseudolatex-membrane for ketoprofen transdermal drug delivery systems, Ind Eng Chem Res. 52 (2013) 15847-15854.

DOI: 10.1021/ie402345a

Google Scholar

[11] R. Waiprib, P. Boonme, W. Taweepreda, E. Kalkornsurapranee, J. Suksaeree, and W. Pichayakorn, Deproteinized natural rubber latex/gelatinized starch blended films as drug delivery carrier, Monatsh Chem Chem Mon. 148 (2017) 1223-1228.

DOI: 10.1007/s00706-017-2005-x

Google Scholar

[12] H. Dias Murbach, G. Jaques Ogawa, F. Azevedo Borges, M.C. Romeiro Miranda, R. Lopes, N. Roberto de Barros, A.V. Guedes Mazalli, R. Gonçalves da Silva, J.L. Ferreira Cinman, B. de Camargo Drago, and R. Donizetti Herculano, Ciprofloxacin release using natural rubber latex membranes as carrier, Int J Biomat. 2014 (2014) 1-7.

DOI: 10.1155/2014/157952

Google Scholar

[13] M. Guyot and F. Fawaz, Design and in vitro evaluation of adhesive matrix for transdermal delivery of propranolol, Int J Pharm. 204 (2000) 171-182.

DOI: 10.1016/s0378-5173(00)00494-4

Google Scholar

[14] P. Costa and J.M.S. Lobo, Modeling and comparison of dissolution profiles, Eur J Pharm Sci. 13 (2001) 123-133.

Google Scholar

[15] Organization for Economic Co-operation and Development (OECD), OECD Guidelines for Testing of Chemicals, Section 4: Health Effects, Test No. 404: Acute Dermal Irritation/Corrosion. Paris Cedex 162002.

DOI: 10.1787/9789264242678-en

Google Scholar

[16] J.H. Draize, G. Woodard, and H.O. Calvery, Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous membranes, J Pharm Exp Therap. 82 (1944) 377-390.

Google Scholar