scholarly journals EVALUASI IN VITRO-IN VIVO FILM TRANDERMAL DILTIAZEM HCL DENGAN PENINGKAT PENETRASI PEG 400 SEBAGAI ANTIHIPERTENSI

2019 ◽  
Vol 16 (01) ◽  
pp. 1
Author(s):  
Yulias Ninik Windriyati ◽  
Risha Fillah Fithria ◽  
Fitria Dwi Kurniawati ◽  
Ulfa Risalatul Mukaromah

ABSTRACTDiltiazem HCL is an antihypertensive that low oral bioavailability of 40%, so developed to transdermal preparations. A matrix type of transdermal patch of diltiazem HCl was prepared using polyvinyl alcohol and ethyl cellulose with PEG 400 as penetration enhancer. In vitro-in vivo evaluation were conducted to asses drug permeation through the skin and determine the effectiveness of transdermal film as an antihypertensive drug. Transdermal patches of diltiazem HCl were evaluated for physicochemical characteristics weight variation, thickness, folding endurance, moisture uptake, and drug content. In vitro permeation study was conducted using commercial semi permeable membrane in Franz diffusion cell. In vivo activity study was evaluated on male rat Wistar that induced NaCl with CODA non-invasive blood pressure method. Transdermal patches of diltiazem HCl were found no significant differences in terms of physicochemical characteristics. The in vitro skin permeation profiles showed increased flux values with the increase of PEG 400 as a penetration enhancer. The in vivo evaluation showed a reduction in systolic and diastolic blood pressure within one hour after the drug administration. Diltiazem HCl was able penetration into skin, absorbed in blood circulation and effective as antihypertensive via transdermal route.Keywords : antihypertension, diltiazem HCl, PEG 400, transdermal patch

2017 ◽  
Vol 12 (2) ◽  
Author(s):  
Kalpana G. Patel ◽  
Vaishali T. Thakkar ◽  
Kartik H. Dudhat ◽  
Mitesh H. Motisariya ◽  
Purvi A. Shah ◽  
...  

2016 ◽  
Vol 18 (3) ◽  
pp. 738-748 ◽  
Author(s):  
Tingting Pu ◽  
Xiaohui Li ◽  
Yuming Sun ◽  
Xue Ding ◽  
Yaqing Pan ◽  
...  

2014 ◽  
Vol 47 (4) ◽  
pp. 49-58
Author(s):  
Mamatha Tirunagari ◽  
Venkateswara Rao Jangala ◽  
Anitha Nandagopal

2019 ◽  
Vol 114 ◽  
pp. 108770 ◽  
Author(s):  
Bhakti Sadarani ◽  
Anuradha Majumdar ◽  
Shalaka Paradkar ◽  
Anupam Mathur ◽  
Satbir Sachdev ◽  
...  

2021 ◽  
Vol 11 (5) ◽  

The present study was aimed at the formulation of transdermal patches of flupirtine maleate containing different permeation enhancers. It acts indirectly as N-methyl-D-aspartate (NMDA) receptor antagonist and activates the K+ channels; thereby acts as a skeletal muscle relaxant. Flupirtine maleate transdermal patches are intended to provide localized effect. The patches were prepared by solvent evaporation technique, using polyvinyl alcohol (PVA) as the polymer whereas dimethyl sulfoxide (DMSO) and polyethylene glycol (PEG-400) as the permeation enhancers. Methanol was used as a solvent to dissolve the drug and glycerol was used as the plasticizer. These patches were evaluated for in vitro permeation, tensile strength, percent moisture absorption, drug content uniformity, film thickness, weight variation and folding endurance. All the patches showed extended release properties. Formulation FDD8 containing 8% polymer and 2% DMSO was found to be the optimized formulation on the basis of evaluation parameters. In vitro permeation release was found to be 95.71 ± 0.01% at the end of 12 h. As the concentration of DMSO increased, the release profile of drug was enhanced. This indicated that DMSO improved the release profile of flupirtine maleate when compared to PEG-400. The release kinetics of the transdermal patches followed Higuchi matrix model. The stability studies showed that all the optimized patches were stable during their study period. From the present study, it can be concluded that addition of DMSO yields good result to enhance the permeation of the drug. Keywords: flupirtine maleate, transdermal patch, permeation enhancers, dimethyl sulfoxide DMSO, polyethylene glycol PEG-400, polyvinyl alcohol PVA.


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