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1.
J Biosci Bioeng ; 134(5): 471-476, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36151004

RESUMO

The structure of the skin only allows those hydrophobic elements to penetrate through the depth of the skin with low molecular weight (less than 500 Da) and low daily dose (less than 100 mg/day). Skin penetration of many drugs such as antibiotics at a high daily dose remains an unresolved challenge. In this study a transdermal patch using cephalexin as an antibiotic drug model was developed. Cephalexin was loaded into α-tocopherol succinate-based solid lipid nanoparticles (SLNs). Cephalexin-loaded SLNs with a drug/lipid ratio of 20%, diameter of 180 ± 7 nm, and drug loading 7.9% led to the greatest inhibition zone of Staphylococcus aureus and showed the highest skin permeation capabilities. Cephalexin-loaded SLNs were distributed into poly-iso-butylene adhesive solution and final patches prepared using solvent casting. The physico-chemical characteristics, in vitro drug release, antimicrobial efficacy, and skin cell proliferation properties of patches were evaluated. Results indicated that the optimal transdermal patch formulation containing 90% adhesive solution, 7% cephalexin, and 3% cephalexin-loaded SLNs (with antibiotic content approximately 28% less) inhibited growth of S.aureus better than the formulation containing 90% adhesive solution and 10% cephalexin. In vitro evaluation of the growth of human fibroblast skin cells in media with the optimal patch exhibited greater proliferation (about 25.5%) than those in media without the patch.


Assuntos
Nanopartículas , Adesivo Transdérmico , Humanos , Absorção Cutânea , Administração Cutânea , Adesivos/química , Adesivos/metabolismo , Antibacterianos/metabolismo , Nanopartículas/química , Pele/metabolismo , Liberação Controlada de Fármacos , Cefalexina/metabolismo , Portadores de Fármacos/química
2.
AAPS PharmSciTech ; 11(1): 278-84, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20182829

RESUMO

In this study, some single-layer and double-layer transdermal drug delivery systems (TDDSs) with different functional and non-functional acrylic pressure-sensitive adhesives (PSAs) were prepared. For this purpose, fentanyl as a drug was used. The effects of PSAs type, single-layer and double-layer TDDSs on skin permeation and in vitro drug release from devices were evaluated using a hydrodynamically well-characterized Chien permeation system fitted with excised rat abdominal skin. The adhesion properties of devices such as peel strength and tack values were obtained as well. It was found that TDDS with -COOH functional PSA showed the lowest steady-state flux. Double-layer TDDS displayed a constant flux up to 72 h. In double- and single-layer devices after 1 and 3 h, respectively, drug release followed Higuchi's kinetic model. Formulations with the highest percentage of -COOH functional PSA have displayed the lowest flux. The double-layer TDDSs with non-functional PSA demonstrated the suitable skin permeation rate close to Duragesic(R) TDDS and suitable adhesion properties.


Assuntos
Adesivos/metabolismo , Fentanila/metabolismo , Pele/metabolismo , Administração Cutânea , Animais , Formas de Dosagem , Excipientes/metabolismo , Masculino , Pressão , Ratos , Ratos Sprague-Dawley
3.
Drug Dev Ind Pharm ; 35(4): 487-98, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19043820

RESUMO

In this study, the influence of the ratio of silicone (Si) to acrylic pressure-sensitive adhesive (PSA), polyvinyl pyrrolidone (PVP), and lauryl alcohol (LA) % (wt/wt) on the properties of a drug in adhesive patch containing 4% (wt/wt) fentanyl as model drug was evaluated. The dependent variables selected were drug solubility, in vitro drug release in the platforms as well as adhesion properties including peel strength and tack value. By using the central composite design of Design Expert software, it was found that the effect of each factor was different, yet all had influenced dependent variables significantly (p < .05). Quadratic model generated for various response variables using backward regression analysis was found to be statistically significant (p < .05). It was deduced that the presence of PVP and Si displayed similar trends on drug solubility and release. Each role played by Si with LA and PVP in release rate was separately investigated, and it was found that the presence of PVP and LA in lowering the amount of drug released was more dominant compared with that of Si. The release patterns at the early and later stages follow the Higuchi and semiempirical models, respectively. Effect of PVP as well as Si and LA were similar on tack value. The influence of LA compared to peeling characteristics of Si system was more pronounced.


Assuntos
Acrilatos/química , Adesivos/química , Analgésicos Opioides/química , Fentanila/química , Silicones/química , Administração Cutânea , Química Farmacêutica , Físico-Química , Preparações de Ação Retardada , Difusão , Dodecanol/química , Sistemas de Liberação de Medicamentos , Cinética , Teste de Materiais , Polienos/química , Polímeros/química , Povidona/química , Solubilidade
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