In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion

Periodontitis, a biofilm infection affecting the gum and teeth, has a high prevalence and has no efficient treatment to date. In this study, doxycycline hyclate, a semi synthetic derivative of tetracycline was used as the active pharmaceutical ingredient (API) to formulate an anti-periodontitis e...

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Main Authors: Mohd Shafri, Mohd Affendi, Mohamed, Farahidah, Hamidon, Nurhani Emira, Adina, Anugerah Budipratama
Format: Proceeding Paper
Language:English
English
Published: 2017
Subjects:
Online Access:http://irep.iium.edu.my/71912/
http://irep.iium.edu.my/71912/7/71912%20In-vitro%20Release%20Profile.pdf
http://irep.iium.edu.my/71912/1/poster%20IABS%202017%20%281%29.pdf
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author Mohd Shafri, Mohd Affendi
Mohamed, Farahidah
Hamidon, Nurhani Emira
Adina, Anugerah Budipratama
author_facet Mohd Shafri, Mohd Affendi
Mohamed, Farahidah
Hamidon, Nurhani Emira
Adina, Anugerah Budipratama
author_sort Mohd Shafri, Mohd Affendi
building IIUM Repository
collection Online Access
description Periodontitis, a biofilm infection affecting the gum and teeth, has a high prevalence and has no efficient treatment to date. In this study, doxycycline hyclate, a semi synthetic derivative of tetracycline was used as the active pharmaceutical ingredient (API) to formulate an anti-periodontitis emulsion. Different amount of lecithin and hydroxypropylmethylcellulose (HPMC), both acting as surfactants, were used in the formulations and tested for drug release profile. The in-vitro drug release profile was conducted using USP Apparatus 1 with PBS of pH 6.8 under sink condition. A predetermined time point h0was set up to take out the solution from the vessel for quantification. In order to quantify the in-vitro performance, a method validation was completed using UV-spectrophotometry following the requirements listed under ICH Q2 (R1) guidelines. A standard calibration curve with a good linearity, R2= 0.9973 was established. LOD and LOQ were in the range of 0.009 and 0.027 µg/mL respectively, whereas the slope of the standard curve was 0.051. The recovery rate for intra-day was from 98.27 to 101.39%, and from 100.85 to 102.57% for inter-day. The RSD was 1.6. It was found that lecithin-added formulation showsed complete drug release after 5 hours. In contrast, lecithin+HPMC-added formulation gave a total release after 2 hours. Thus, the lecithin-added formulation showed a slower release profile compared to the lecithin+HPMC-added formulation and may be the formulation of choice for future testings.
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format Proceeding Paper
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institution International Islamic University Malaysia
institution_category Local University
language English
English
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publishDate 2017
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spelling iium-719122019-05-02T08:43:41Z http://irep.iium.edu.my/71912/ In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion Mohd Shafri, Mohd Affendi Mohamed, Farahidah Hamidon, Nurhani Emira Adina, Anugerah Budipratama RS Pharmacy and materia medica Periodontitis, a biofilm infection affecting the gum and teeth, has a high prevalence and has no efficient treatment to date. In this study, doxycycline hyclate, a semi synthetic derivative of tetracycline was used as the active pharmaceutical ingredient (API) to formulate an anti-periodontitis emulsion. Different amount of lecithin and hydroxypropylmethylcellulose (HPMC), both acting as surfactants, were used in the formulations and tested for drug release profile. The in-vitro drug release profile was conducted using USP Apparatus 1 with PBS of pH 6.8 under sink condition. A predetermined time point h0was set up to take out the solution from the vessel for quantification. In order to quantify the in-vitro performance, a method validation was completed using UV-spectrophotometry following the requirements listed under ICH Q2 (R1) guidelines. A standard calibration curve with a good linearity, R2= 0.9973 was established. LOD and LOQ were in the range of 0.009 and 0.027 µg/mL respectively, whereas the slope of the standard curve was 0.051. The recovery rate for intra-day was from 98.27 to 101.39%, and from 100.85 to 102.57% for inter-day. The RSD was 1.6. It was found that lecithin-added formulation showsed complete drug release after 5 hours. In contrast, lecithin+HPMC-added formulation gave a total release after 2 hours. Thus, the lecithin-added formulation showed a slower release profile compared to the lecithin+HPMC-added formulation and may be the formulation of choice for future testings. 2017 Proceeding Paper NonPeerReviewed application/pdf en http://irep.iium.edu.my/71912/7/71912%20In-vitro%20Release%20Profile.pdf application/pdf en http://irep.iium.edu.my/71912/1/poster%20IABS%202017%20%281%29.pdf Mohd Shafri, Mohd Affendi and Mohamed, Farahidah and Hamidon, Nurhani Emira and Adina, Anugerah Budipratama (2017) In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion. In: 2nd International Anatomical and Biomedical Scientific Conference 2017 (IABS), 1st-2nd August 2017, Serdang, Selangor. (Unpublished)
spellingShingle RS Pharmacy and materia medica
Mohd Shafri, Mohd Affendi
Mohamed, Farahidah
Hamidon, Nurhani Emira
Adina, Anugerah Budipratama
In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title_full In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title_fullStr In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title_full_unstemmed In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title_short In-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
title_sort in-vitro release profile of anti-periodontitis doxycycline hyclate emulsion
topic RS Pharmacy and materia medica
url http://irep.iium.edu.my/71912/
http://irep.iium.edu.my/71912/7/71912%20In-vitro%20Release%20Profile.pdf
http://irep.iium.edu.my/71912/1/poster%20IABS%202017%20%281%29.pdf