<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml"><p>Buccal patches of salbutamol sulfate were prepared using five different water soluble polymers in various proportions and combinations using PEG-400/PG as plasticizers. A 3<sup>2</sup> full factorial design was used to design the experiments for each polymer combination. Patches were laminated on one side with a water impermeable backing layer for unidirectional drug release. The thickness of medicated patches ranged between 0.2 and 0.4 mm and showed an increase in mass whenever PEG-400 was used as plasticizer. The surface pH of all patches approached neutral. Eight formulations which had shown high folding endurance (> 300) were selected for evaluation. Patches prepared with PEG-400 showed a high swelling index. The residence time of the tested patches ranged between 105 and 130 min. Formulations A10, A32, B10 and B32 fitted the Higuchi model best, whereas formulations A19 and B19 showed super case II transport drug release. Stability studies indicated that there was no change in the chemical and physical characteristics during the test period of 6 months.</p></abstract>

Buccal patches of salbutamol sulfate were prepared using five different water soluble polymers in various proportions and combinations using PEG-400/PG as plasticizers. A 32 full factorial design was used to design the experiments for each polymer combination. Patches were laminated on one side with a water impermeable backing layer for unidirectional drug release. The thickness of medicated patches ranged between 0.2 and 0.4 mm and showed an increase in mass whenever PEG-400 was used as plasticizer. The surface pH of all patches approached neutral. Eight formulations which had shown high folding endurance (> 300) were selected for evaluation. Patches prepared with PEG-400 showed a high swelling index. The residence time of the tested patches ranged between 105 and 130 min. Formulations A10, A32, B10 and B32 fitted the Higuchi model best, whereas formulations A19 and B19 showed super case II transport drug release. Stability studies indicated that there was no change in the chemical and physical characteristics during the test period of 6 months.

Development and characterization of mucoadhesive patches of salbutamol sulfate for unidirectional buccal drug delivery

Department of Pharmaceutical Technology, Anna University of Technology, Tiruchirapalli, Tiruchirapalli 620 024, India

Department of Pharmaceutics, Gautham College of Pharmacy, Sultanpalya, Bangalore, 560 032 India

Document Operations in Clinical, Novartis Health Care Pvt Ltd., Hyderabad, 500 072, India

Department of Pharmaceutical Chemistry, Jadavpur University, Kolkata, 700 032, India

Acta Pharmaceutica

Buccal patches of salbutamol sulfate were prepared using five different water soluble polymers in various proportions and combinations using PEG-400/PG as...

Development and characterization of mucoadhesive patches of salbutamol sulfate for unidirectional buccal drug delivery

Data publikacji: 17 cze 2011

Zakres stron: 157 - 170

DOI: https://doi.org/10.2478/v10007-011-0011-9

Słowa kluczowe
salbutamol sulfat, mukoadhezivni flasteri, bukalna isporuka, 3 potpuni faktorijalni dizajn

This content is open access.

Development and characterization of mucoadhesive patches of salbutamol sulfate for unidirectional buccal drug delivery

Data publikacji: 17 cze 2011

Zakres stron: 157 - 170

DOI: https://doi.org/10.2478/v10007-011-0011-9

Słowa kluczowesalbutamol sulfat, mukoadhezivni flasteri, bukalna isporuka, 3 potpuni faktorijalni dizajn

This content is open access.

Słowa kluczowe
salbutamol sulfat, mukoadhezivni flasteri, bukalna isporuka, 3 potpuni faktorijalni dizajn