Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent
Chitosan and gelatin were used as polymer scaffolds for cartilage tissue engineering. The scaffold was used as a biodegradable drug delivery system for diclofenac sodium to treat cartilage defects on osteoarthritis (OA). The materials were composed of diclofenac sodium, chitosan, gelatin, and cross-...
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id-langga.1196682023-02-01T03:11:25Z https://repository.unair.ac.id/119668/ Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent Aniek Setiya Budiatin, - Nily Su’aida, - Aziszia Insanya Lamakluang, - Silda Sabila Rahma, - Bambang Subakti Zulkarnain, - Dewi Isadiartuti, - R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica RS200-201 Pharmaceutical dosage forms Chitosan and gelatin were used as polymer scaffolds for cartilage tissue engineering. The scaffold was used as a biodegradable drug delivery system for diclofenac sodium to treat cartilage defects on osteoarthritis (OA). The materials were composed of diclofenac sodium, chitosan, gelatin, and cross-linking agent-glutaraldehyde (GTA) were form as scaffold. The purpose of this study to investigate the effect of GTA concentration variations (0.00%; 0.25%; 0.50%; 1.00%; 2.50%) on characteristics and the release of diclofenac sodium from chitosan-gelatin scaffold. The scaffolds were made by using the pre-freezing method with a temperature of -56 ± 5°C for 24 hours and characterized by porosity, pore size, swelling, degradation, toxicity test, and diclofenac sodium released from chitosan-gelatin scaffolds at pH and temperature body. The results showed, the addition of GTA increased the swelling ratio from 195.79 ± 7.04% to 793.49 ± 6.92% and minimized weight loss up to 50.98 ± 0.82%, percentage of living cells >60%, optimal porosity at 106.94 ± 9.38 % with pore size 135.48 ± 89.70 µm, diclofenac sodium as sustained release drug completed in 542 hours and the release was following zero-order kinetic. Chitosan-gelatin scaffold is a potential candidate for cartilage tissue engineering and drug delivery system for diclofenac sodium. A and V Publication 2022-11-24 Article PeerReviewed text en https://repository.unair.ac.id/119668/1/C-13%20Artikel%20dan%20SJR_001.pdf text en https://repository.unair.ac.id/119668/2/C-13%20Validasi%20Kadep%20dan%20Kualitas%20Karil_001.pdf text en https://repository.unair.ac.id/119668/3/C-13%20Similarity_001.pdf text en https://repository.unair.ac.id/119668/7/C-13%20Korespondensi.pdf Aniek Setiya Budiatin, - and Nily Su’aida, - and Aziszia Insanya Lamakluang, - and Silda Sabila Rahma, - and Bambang Subakti Zulkarnain, - and Dewi Isadiartuti, - (2022) Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent. Research Journal of Pharmacy and Technology, 15 (11). pp. 4974-4980. ISSN 0974-3618 https://www.rjptonline.org/HTMLPaper.aspx?Journal=Research%20Journal%20of%20Pharmacy%20and%20Technology;PID=2022-15-11-21 https://doi.org/10.52711/0974-360X.2022.00836 |
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R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica RS200-201 Pharmaceutical dosage forms Aniek Setiya Budiatin, - Nily Su’aida, - Aziszia Insanya Lamakluang, - Silda Sabila Rahma, - Bambang Subakti Zulkarnain, - Dewi Isadiartuti, - Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
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Chitosan and gelatin were used as polymer scaffolds for cartilage tissue engineering. The scaffold was used as a biodegradable drug delivery system for diclofenac sodium to treat cartilage defects on osteoarthritis (OA). The materials were composed of diclofenac sodium, chitosan, gelatin, and cross-linking agent-glutaraldehyde (GTA) were form as scaffold. The purpose of this study to investigate the effect of GTA concentration variations (0.00%; 0.25%; 0.50%; 1.00%; 2.50%) on characteristics and the release of diclofenac sodium from chitosan-gelatin scaffold. The scaffolds were made by using the pre-freezing method with a temperature of -56 ± 5°C for 24 hours and characterized by porosity, pore size, swelling, degradation, toxicity test, and diclofenac sodium released from chitosan-gelatin scaffolds at pH and temperature body. The results showed, the addition of GTA increased the swelling ratio from 195.79 ± 7.04% to 793.49 ± 6.92% and minimized weight loss up to 50.98 ± 0.82%, percentage of living cells >60%, optimal porosity at 106.94 ± 9.38 % with pore size 135.48 ± 89.70 µm, diclofenac sodium as sustained release drug completed in 542 hours and the release was following zero-order kinetic. Chitosan-gelatin scaffold is a potential candidate for cartilage tissue engineering and drug delivery system for diclofenac sodium. |
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Article PeerReviewed |
author |
Aniek Setiya Budiatin, - Nily Su’aida, - Aziszia Insanya Lamakluang, - Silda Sabila Rahma, - Bambang Subakti Zulkarnain, - Dewi Isadiartuti, - |
author_facet |
Aniek Setiya Budiatin, - Nily Su’aida, - Aziszia Insanya Lamakluang, - Silda Sabila Rahma, - Bambang Subakti Zulkarnain, - Dewi Isadiartuti, - |
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Aniek Setiya Budiatin, - |
title |
Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
title_short |
Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
title_full |
Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
title_fullStr |
Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
title_full_unstemmed |
Effect of Glutaraldehyde Concentration Variation on Diclofenac Sodium Scaffolds as Cross-Linking Agent |
title_sort |
effect of glutaraldehyde concentration variation on diclofenac sodium scaffolds as cross-linking agent |
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A and V Publication |
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2022 |
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https://repository.unair.ac.id/119668/1/C-13%20Artikel%20dan%20SJR_001.pdf https://repository.unair.ac.id/119668/2/C-13%20Validasi%20Kadep%20dan%20Kualitas%20Karil_001.pdf https://repository.unair.ac.id/119668/3/C-13%20Similarity_001.pdf https://repository.unair.ac.id/119668/7/C-13%20Korespondensi.pdf https://repository.unair.ac.id/119668/ https://www.rjptonline.org/HTMLPaper.aspx?Journal=Research%20Journal%20of%20Pharmacy%20and%20Technology;PID=2022-15-11-21 https://doi.org/10.52711/0974-360X.2022.00836 |
_version_ |
1757049656199610368 |