In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations

The micelles/liposome formulation for the first time has been constructed via thin-film hydration method containing soy lecithin (L), tween 80 (T), squalene (S), and polyvinyl alcohol (P) (LTSP nanoparticles). Similar ingredients except for lecithin were used for preparing micellar/niosomal vesicula...

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Main Authors: Mohammad Javed Ansari, Mohammed F. Aldawsari, Ameeduzzafar Zafar, Alireza Soltani, Mohd Yasir, Mohammed Asadullah Jahangir, Mohamad Taleuzzaman, Vahid Erfani-Moghadam, Leila Daneshmandi, Nosrat O Mahmoodi, Asieh Yahyazadeh, Md Lutfor Rahman, Mohd Sani Sarjadi
Format: Article
Language:English
English
Published: Elsevier B.V. 2022
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Online Access:https://eprints.ums.edu.my/id/eprint/32639/1/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar.pdf
https://eprints.ums.edu.my/id/eprint/32639/2/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar1.pdf
https://eprints.ums.edu.my/id/eprint/32639/
https://www.sciencedirect.com/science/article/pii/S1110016822001089
https://doi.org/10.1016/j.aej.2022.02.019
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Institution: Universiti Malaysia Sabah
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spelling my.ums.eprints.326392022-05-20T00:40:56Z https://eprints.ums.edu.my/id/eprint/32639/ In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations Mohammad Javed Ansari Mohammed F. Aldawsari Ameeduzzafar Zafar Alireza Soltani Mohd Yasir Mohammed Asadullah Jahangir Mohamad Taleuzzaman Vahid Erfani-Moghadam Leila Daneshmandi Nosrat O Mahmoodi Asieh Yahyazadeh Md Lutfor Rahman Mohd Sani Sarjadi QD1-999 Chemistry The micelles/liposome formulation for the first time has been constructed via thin-film hydration method containing soy lecithin (L), tween 80 (T), squalene (S), and polyvinyl alcohol (P) (LTSP nanoparticles). Similar ingredients except for lecithin were used for preparing micellar/niosomal vesicular SSZ nano formulation (TSP nanoparticles). The percent drug loading and encapsulation efficiency of SSZ was 7.39% and 98.5 ± 0.3 % for the 7.5:100 (w/w) ratio of SSZ: total weight of LTSP, while the percent drug loading and encapsulation efficiency of SSZ was 4.7% and 62.85 ± 0.3 % in the TSP nano formulation. Dynamic light scattering (DLS) and trans- mission electron microscopy (TEM) results showed that both formulations formed spherical micelles and vesicles with globule sizes of 25 ± 1.2 nm and 100 ± 20.5 nm respectively. The cell toxicity evaluations showed that both LTSP and TSP nano formulations without drug were nontoxic (at the range of this experiment) for Human Dermal Fibroblasts (HDF) as a normal cell line, but SSZ loaded nano formulation exhibited increased cell toxicity with half-maximal inhibitory concentration (IC50) of 940 mM for SSZ alone to near 240 mM for SSZ loaded nano formulation (approximately four times). In vitro release experiments exhibited sustained release of SSZ from both nano formulations. The LTSP micellar/liposomal and TSP micellar/niosomal nano formulation for SSZ delivery can be considered as appropriate approaches for improving its bioavailability and probably they are good candidates for future clinical investigations. Elsevier B.V. 2022 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/32639/1/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar.pdf text en https://eprints.ums.edu.my/id/eprint/32639/2/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar1.pdf Mohammad Javed Ansari and Mohammed F. Aldawsari and Ameeduzzafar Zafar and Alireza Soltani and Mohd Yasir and Mohammed Asadullah Jahangir and Mohamad Taleuzzaman and Vahid Erfani-Moghadam and Leila Daneshmandi and Nosrat O Mahmoodi and Asieh Yahyazadeh and Md Lutfor Rahman and Mohd Sani Sarjadi (2022) In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations. Alexandria Engineering Journal, 61. pp. 9749-9756. ISSN 1110-0168 https://www.sciencedirect.com/science/article/pii/S1110016822001089 https://doi.org/10.1016/j.aej.2022.02.019
institution Universiti Malaysia Sabah
building UMS Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sabah
content_source UMS Institutional Repository
url_provider http://eprints.ums.edu.my/
language English
English
topic QD1-999 Chemistry
spellingShingle QD1-999 Chemistry
Mohammad Javed Ansari
Mohammed F. Aldawsari
Ameeduzzafar Zafar
Alireza Soltani
Mohd Yasir
Mohammed Asadullah Jahangir
Mohamad Taleuzzaman
Vahid Erfani-Moghadam
Leila Daneshmandi
Nosrat O Mahmoodi
Asieh Yahyazadeh
Md Lutfor Rahman
Mohd Sani Sarjadi
In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
description The micelles/liposome formulation for the first time has been constructed via thin-film hydration method containing soy lecithin (L), tween 80 (T), squalene (S), and polyvinyl alcohol (P) (LTSP nanoparticles). Similar ingredients except for lecithin were used for preparing micellar/niosomal vesicular SSZ nano formulation (TSP nanoparticles). The percent drug loading and encapsulation efficiency of SSZ was 7.39% and 98.5 ± 0.3 % for the 7.5:100 (w/w) ratio of SSZ: total weight of LTSP, while the percent drug loading and encapsulation efficiency of SSZ was 4.7% and 62.85 ± 0.3 % in the TSP nano formulation. Dynamic light scattering (DLS) and trans- mission electron microscopy (TEM) results showed that both formulations formed spherical micelles and vesicles with globule sizes of 25 ± 1.2 nm and 100 ± 20.5 nm respectively. The cell toxicity evaluations showed that both LTSP and TSP nano formulations without drug were nontoxic (at the range of this experiment) for Human Dermal Fibroblasts (HDF) as a normal cell line, but SSZ loaded nano formulation exhibited increased cell toxicity with half-maximal inhibitory concentration (IC50) of 940 mM for SSZ alone to near 240 mM for SSZ loaded nano formulation (approximately four times). In vitro release experiments exhibited sustained release of SSZ from both nano formulations. The LTSP micellar/liposomal and TSP micellar/niosomal nano formulation for SSZ delivery can be considered as appropriate approaches for improving its bioavailability and probably they are good candidates for future clinical investigations.
format Article
author Mohammad Javed Ansari
Mohammed F. Aldawsari
Ameeduzzafar Zafar
Alireza Soltani
Mohd Yasir
Mohammed Asadullah Jahangir
Mohamad Taleuzzaman
Vahid Erfani-Moghadam
Leila Daneshmandi
Nosrat O Mahmoodi
Asieh Yahyazadeh
Md Lutfor Rahman
Mohd Sani Sarjadi
author_facet Mohammad Javed Ansari
Mohammed F. Aldawsari
Ameeduzzafar Zafar
Alireza Soltani
Mohd Yasir
Mohammed Asadullah Jahangir
Mohamad Taleuzzaman
Vahid Erfani-Moghadam
Leila Daneshmandi
Nosrat O Mahmoodi
Asieh Yahyazadeh
Md Lutfor Rahman
Mohd Sani Sarjadi
author_sort Mohammad Javed Ansari
title In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
title_short In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
title_full In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
title_fullStr In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
title_full_unstemmed In vitro release and cytotoxicity study of encapsulated sulfasalazine within LTSP micellar/ liposomal and TSP micellar/niosomal nano-formulations
title_sort in vitro release and cytotoxicity study of encapsulated sulfasalazine within ltsp micellar/ liposomal and tsp micellar/niosomal nano-formulations
publisher Elsevier B.V.
publishDate 2022
url https://eprints.ums.edu.my/id/eprint/32639/1/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar.pdf
https://eprints.ums.edu.my/id/eprint/32639/2/In%20vitro%20release%20and%20cytotoxicity%20study%20of%20encapsulated%20sulfasalazine%20within%20LTSP%20micellar1.pdf
https://eprints.ums.edu.my/id/eprint/32639/
https://www.sciencedirect.com/science/article/pii/S1110016822001089
https://doi.org/10.1016/j.aej.2022.02.019
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