Formulation and evaluation of buccal films of piroxicam co-crystals
Abstract Background The aim of the present study was to enhance the solubility of piroxicam (BCS class II drug) using co-crystallization technique and formulate the buccal films of selected co-crystals for improved therapeutic utilization of drug. Co-crystals of drug with various co-formers (molar r...
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Online Access: | http://link.springer.com/article/10.1186/s43094-020-00033-1 |
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doaj-632ee4c8490648a9b7b112d53800e19c2020-11-25T02:51:34ZengSpringerOpenFuture Journal of Pharmaceutical Sciences2314-72532020-05-016111110.1186/s43094-020-00033-1Formulation and evaluation of buccal films of piroxicam co-crystalsAnand Ammanage0Paul Rodriques1Amolkumar Kempwade2Ravindra Hiremath3KLES College of PharmacyKLES College of PharmacyKLES College of PharmacyKLES College of PharmacyAbstract Background The aim of the present study was to enhance the solubility of piroxicam (BCS class II drug) using co-crystallization technique and formulate the buccal films of selected co-crystals for improved therapeutic utilization of drug. Co-crystals of drug with various co-formers (molar ratio 1:1) were prepared by solvent evaporation method and were screened for their aqueous solubility and percent drug content. The formation of co-crystals was confirmed by FTIR, DSC and XRD. Piroxicam co-crystals loaded buccal films were prepared and evaluated for in vitro drug release, ex vivo drug permeation while safety of formulation was determined by histopathological study. Results The co-crystals prepared with different co-formers have proved their potential to improve the solubility of the drug. Co-crystals of piroxicam-sucralose have shown six-folds more solubility than parent drug. FTIR analysis indicated shifting in characteristics peaks of piroxicam. DSC analysis showed an extra exothermic peak and alteration in characteristic endothermic peak. The powder x-ray diffraction pattern exhibited changes in 2θ values of intense peaks. Thus, formation of co-crystal was confirmed. Physical characters of buccal films were found to be within limits. Formulation F6 showed highest mucoadhesive strength (5617 ± 636 dynes /cm2) while formulation F2 showed highest in vitro drug release after 8 h, i.e., 94.557%. The ex vivo drug permeation of F2 was found to be 84.74%. The hisopathological study revealed that there was no damage to buccal mucosal tissue and was found to be intact. Conclusion The piroxicam-suralose co-crystals based mucoadhesive films of piroxicam could be a better formulation approach with improved solubility, safety, and therapeutic efficacy as compared to conventional tablets. Graphical abstracthttp://link.springer.com/article/10.1186/s43094-020-00033-1PiroxicamSucraloseCo-crystalsMucoadhesiveBuccal film |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anand Ammanage Paul Rodriques Amolkumar Kempwade Ravindra Hiremath |
spellingShingle |
Anand Ammanage Paul Rodriques Amolkumar Kempwade Ravindra Hiremath Formulation and evaluation of buccal films of piroxicam co-crystals Future Journal of Pharmaceutical Sciences Piroxicam Sucralose Co-crystals Mucoadhesive Buccal film |
author_facet |
Anand Ammanage Paul Rodriques Amolkumar Kempwade Ravindra Hiremath |
author_sort |
Anand Ammanage |
title |
Formulation and evaluation of buccal films of piroxicam co-crystals |
title_short |
Formulation and evaluation of buccal films of piroxicam co-crystals |
title_full |
Formulation and evaluation of buccal films of piroxicam co-crystals |
title_fullStr |
Formulation and evaluation of buccal films of piroxicam co-crystals |
title_full_unstemmed |
Formulation and evaluation of buccal films of piroxicam co-crystals |
title_sort |
formulation and evaluation of buccal films of piroxicam co-crystals |
publisher |
SpringerOpen |
series |
Future Journal of Pharmaceutical Sciences |
issn |
2314-7253 |
publishDate |
2020-05-01 |
description |
Abstract Background The aim of the present study was to enhance the solubility of piroxicam (BCS class II drug) using co-crystallization technique and formulate the buccal films of selected co-crystals for improved therapeutic utilization of drug. Co-crystals of drug with various co-formers (molar ratio 1:1) were prepared by solvent evaporation method and were screened for their aqueous solubility and percent drug content. The formation of co-crystals was confirmed by FTIR, DSC and XRD. Piroxicam co-crystals loaded buccal films were prepared and evaluated for in vitro drug release, ex vivo drug permeation while safety of formulation was determined by histopathological study. Results The co-crystals prepared with different co-formers have proved their potential to improve the solubility of the drug. Co-crystals of piroxicam-sucralose have shown six-folds more solubility than parent drug. FTIR analysis indicated shifting in characteristics peaks of piroxicam. DSC analysis showed an extra exothermic peak and alteration in characteristic endothermic peak. The powder x-ray diffraction pattern exhibited changes in 2θ values of intense peaks. Thus, formation of co-crystal was confirmed. Physical characters of buccal films were found to be within limits. Formulation F6 showed highest mucoadhesive strength (5617 ± 636 dynes /cm2) while formulation F2 showed highest in vitro drug release after 8 h, i.e., 94.557%. The ex vivo drug permeation of F2 was found to be 84.74%. The hisopathological study revealed that there was no damage to buccal mucosal tissue and was found to be intact. Conclusion The piroxicam-suralose co-crystals based mucoadhesive films of piroxicam could be a better formulation approach with improved solubility, safety, and therapeutic efficacy as compared to conventional tablets. Graphical abstract |
topic |
Piroxicam Sucralose Co-crystals Mucoadhesive Buccal film |
url |
http://link.springer.com/article/10.1186/s43094-020-00033-1 |
work_keys_str_mv |
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