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Search results for: mucoadhesiveness
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style="font-size:1.6rem;">Search results for: mucoadhesiveness</h1> <div class="card publication-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2</span> In vitro Studies of Mucoadhesiveness and Release of Nicotinamide Oral Gels Prepared from Bioadhesive Polymers</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/search?q=Sarunyoo%20Songkro">Sarunyoo Songkro</a>, <a href="https://publications.waset.org/search?q=Naranut%20Rajatasereekul"> Naranut Rajatasereekul</a>, <a href="https://publications.waset.org/search?q=Nipapat%20Cheewasrirungrueng"> Nipapat Cheewasrirungrueng</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The aim of the present study was to evaluate the mucoadhesion and the release of nicotinamide gel formulations using in vitro methods. An agar plate technique was used to investigate the adhesiveness of the gels whereas a diffusion apparatus was employed to determine the release of nicotinamide from the gels. In this respect, 10% w/w nicotinamide gels containing bioadhesive polymers: Carbopol 934P (0.5-2% w/w), hydroxypropylmethyl cellulose (HPMC) (4-10% w/w), sodium carboxymethyl cellulose (SCMC) (4-6% w/w) and methylcellulose 4000 (MC) (3-5% w/w) were prepared. The gel formulations had pH values in the range of 7.14 - 8.17, which were considered appropriate to oral mucosa application. In general, the rank order of pH values appeared to be SCMC > MC4000 > HPMC > Carbopol 934P. Types and concentrations of polymers used somewhat affected the adhesiveness. It was found that anionic polymers (Carbopol 934 and SCMC) adhered more firmly to the agar plate than the neutral polymers (HPMC and MC 4000). The formulation containing 0.5% Carbopol 934P (F1) showed the highest release rate. With the exception of the formulation F1, the neutral polymers tended to give higher relate rates than the anionic polymers. For oral tissue treatment, the optimum has to be balanced between the residence time (adhesiveness) of the formulations and the release rate of the drug. The formulations containing the anionic polymers: Carbopol 934P or SCMC possessed suitable physical properties (appearance, pH and viscosity). In addition, for anionic polymer formulations, justifiable mucoadhesive properties and reasonable release rates of nicotinamide were achieved. Accordingly, these gel formulations may be applied for the treatment of oral mucosal lesions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/search?q=Nicotinamide" title="Nicotinamide">Nicotinamide</a>, <a href="https://publications.waset.org/search?q=bioadhesive%20polymer" title=" bioadhesive polymer"> bioadhesive polymer</a>, <a href="https://publications.waset.org/search?q=mucoadhesiveness" title=" mucoadhesiveness"> mucoadhesiveness</a>, <a href="https://publications.waset.org/search?q=release%20rate" title=" release rate"> release rate</a>, <a href="https://publications.waset.org/search?q=gel." title=" gel."> gel.</a> </p> <a href="https://publications.waset.org/11316/in-vitro-studies-of-mucoadhesiveness-and-release-of-nicotinamide-oral-gels-prepared-from-bioadhesive-polymers" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/11316/apa" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">APA</a> <a href="https://publications.waset.org/11316/bibtex" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">BibTeX</a> <a href="https://publications.waset.org/11316/chicago" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">Chicago</a> <a href="https://publications.waset.org/11316/endnote" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">EndNote</a> <a href="https://publications.waset.org/11316/harvard" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">Harvard</a> <a href="https://publications.waset.org/11316/json" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">JSON</a> <a href="https://publications.waset.org/11316/mla" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">MLA</a> <a href="https://publications.waset.org/11316/ris" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">RIS</a> <a href="https://publications.waset.org/11316/xml" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">XML</a> <a href="https://publications.waset.org/11316/iso690" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">ISO 690</a> <a href="https://publications.waset.org/11316.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">2692</span> </span> </div> </div> <div class="card publication-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1</span> Growth Effects of Caffeic Acid and Thioglycolic Acid Modified Chitosans in U937 Cells</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/search?q=Aytekin%20A.O.">Aytekin A.O.</a>, <a href="https://publications.waset.org/search?q=Morimura%20S."> Morimura S.</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chitosan is a biopolymer composed of glucosamine and N-acetyl glucosamine. Solubility and viscosity pose problems in some applications. These problems can be overcome with unique modifications. In this study, firstly, chitosan was modified by caffeic acid and thioglycolic acid, separately. Then, growing effects of these modified polymers was observed in U937 cell line. Caffeic acid is a phenolic compound and its modifications act carcinogenic inhibitors in drugs. Thiolated chitosans are commonly being used for drugdelivery systems in various routes, because of enhancing mucoadhesiveness property. U937 cell line was used model cell for leukaemia. Modifications were achieved by 1 – 15 % binding range. Increasing binding ratios showed higher radical-scavenging activity and reducing cell growth, in compared to native chitosan. Caffeic acid modifications showed higher radical-scavenging activity than thiolated chitosans at the same concentrations. Caffeic acid and thioglycolic acid modifications inhibited growth of U937, effectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/search?q=Chitosan" title="Chitosan">Chitosan</a>, <a href="https://publications.waset.org/search?q=U937%20cell" title=" U937 cell"> U937 cell</a>, <a href="https://publications.waset.org/search?q=caffeic%20acid" title=" caffeic acid"> caffeic acid</a>, <a href="https://publications.waset.org/search?q=thioglycolic%20acid" title=" thioglycolic acid"> thioglycolic acid</a> </p> <a href="https://publications.waset.org/1199/growth-effects-of-caffeic-acid-and-thioglycolic-acid-modified-chitosans-in-u937-cells" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/1199/apa" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">APA</a> <a href="https://publications.waset.org/1199/bibtex" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">BibTeX</a> <a 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