Cargando…
Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan
The study's goal was to create an in situ intrarectal mucoadhesive gel of sumatriptan (SMT) combining mucoadhesive polymer (xyloglucan) and thermosensitive polymers (poloxamer 407 and poloxamer 188) to prolong rectal residence time for treatment of migraines. Nine SMT mucoadhesive rectal in sit...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226710/ https://www.ncbi.nlm.nih.gov/pubmed/37255866 http://dx.doi.org/10.4103/japtr.japtr_603_22 |
_version_ | 1785050629874384896 |
---|---|
author | Kassab, Hanan J. Alkufi, Hussein K. Hussein, Lina S. |
author_facet | Kassab, Hanan J. Alkufi, Hussein K. Hussein, Lina S. |
author_sort | Kassab, Hanan J. |
collection | PubMed |
description | The study's goal was to create an in situ intrarectal mucoadhesive gel of sumatriptan (SMT) combining mucoadhesive polymer (xyloglucan) and thermosensitive polymers (poloxamer 407 and poloxamer 188) to prolong rectal residence time for treatment of migraines. Nine SMT mucoadhesive rectal in situ gel (RIG) formulas were created by mixing poloxamer 407 (18%, 19%, or 20%) with poloxamer 188 (5%), a mucoadhesive polymer at various doses (0.1, 0.2, and 0.3) as well as SMT (25 mg/ml). The prepared suppositories underwent for mucoadhesive force, gelation temperature, and gelation time. When SMT and mucoadhesive polymer were added to the poloxamer mixture, the gelation temperature dropped; however, poloxamer 188 had the opposite effect. These polymers supported the prepared liquids' ability to adhere to mucous membranes and form a strong gel. The transition gelation temperature of the poloxamer solution rose as a result of the addition of poloxamer 188. The findings showed that the formula RIG5 which is composed of poloxamer 407 (19%), poloxamer 188 (5%), and xyloglucan (0.2%) had an ideal transition temperature of 36.33°C, gel strength of 44.66°C, mucoadhesive force of 6409°C, and in vitro drug release of 93.98% over an 8-hour period. In light of this, it can be said that SMT was successfully manufactured as RIG without causing any chemical reaction with its additives. |
format | Online Article Text |
id | pubmed-10226710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-102267102023-05-30 Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan Kassab, Hanan J. Alkufi, Hussein K. Hussein, Lina S. J Adv Pharm Technol Res Original Article The study's goal was to create an in situ intrarectal mucoadhesive gel of sumatriptan (SMT) combining mucoadhesive polymer (xyloglucan) and thermosensitive polymers (poloxamer 407 and poloxamer 188) to prolong rectal residence time for treatment of migraines. Nine SMT mucoadhesive rectal in situ gel (RIG) formulas were created by mixing poloxamer 407 (18%, 19%, or 20%) with poloxamer 188 (5%), a mucoadhesive polymer at various doses (0.1, 0.2, and 0.3) as well as SMT (25 mg/ml). The prepared suppositories underwent for mucoadhesive force, gelation temperature, and gelation time. When SMT and mucoadhesive polymer were added to the poloxamer mixture, the gelation temperature dropped; however, poloxamer 188 had the opposite effect. These polymers supported the prepared liquids' ability to adhere to mucous membranes and form a strong gel. The transition gelation temperature of the poloxamer solution rose as a result of the addition of poloxamer 188. The findings showed that the formula RIG5 which is composed of poloxamer 407 (19%), poloxamer 188 (5%), and xyloglucan (0.2%) had an ideal transition temperature of 36.33°C, gel strength of 44.66°C, mucoadhesive force of 6409°C, and in vitro drug release of 93.98% over an 8-hour period. In light of this, it can be said that SMT was successfully manufactured as RIG without causing any chemical reaction with its additives. Wolters Kluwer - Medknow 2023 2023-04-13 /pmc/articles/PMC10226710/ /pubmed/37255866 http://dx.doi.org/10.4103/japtr.japtr_603_22 Text en Copyright: © 2023 Journal of Advanced Pharmaceutical Technology & Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Kassab, Hanan J. Alkufi, Hussein K. Hussein, Lina S. Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title | Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title_full | Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title_fullStr | Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title_full_unstemmed | Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title_short | Use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
title_sort | use of factorial design in formulation and evaluation of intrarectal in situ gel of sumatriptan |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226710/ https://www.ncbi.nlm.nih.gov/pubmed/37255866 http://dx.doi.org/10.4103/japtr.japtr_603_22 |
work_keys_str_mv | AT kassabhananj useoffactorialdesigninformulationandevaluationofintrarectalinsitugelofsumatriptan AT alkufihusseink useoffactorialdesigninformulationandevaluationofintrarectalinsitugelofsumatriptan AT husseinlinas useoffactorialdesigninformulationandevaluationofintrarectalinsitugelofsumatriptan |