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Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata

The aim of the current study is extraction and isolation of bergenin from Bergenia ciliata and fabrication of pH-sensitive Eudragit(®) L100 (EL100) polymeric nanoparticles (NP) to tackle limitations of solubility. Bergenin-loaded EL100 nanoparticles (BN-NP) were fabricated via nanoprecipitation and...

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Autores principales: Bashir, Kashaf, Khan, Muhammad Farhan Ali, Alhodaib, Aiyeshah, Ahmed, Naveed, Naz, Iffat, Mirza, Bushra, Tipu, Muhammad Khalid, Fatima, Humaira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104231/
https://www.ncbi.nlm.nih.gov/pubmed/35566808
http://dx.doi.org/10.3390/polym14091639
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author Bashir, Kashaf
Khan, Muhammad Farhan Ali
Alhodaib, Aiyeshah
Ahmed, Naveed
Naz, Iffat
Mirza, Bushra
Tipu, Muhammad Khalid
Fatima, Humaira
author_facet Bashir, Kashaf
Khan, Muhammad Farhan Ali
Alhodaib, Aiyeshah
Ahmed, Naveed
Naz, Iffat
Mirza, Bushra
Tipu, Muhammad Khalid
Fatima, Humaira
author_sort Bashir, Kashaf
collection PubMed
description The aim of the current study is extraction and isolation of bergenin from Bergenia ciliata and fabrication of pH-sensitive Eudragit(®) L100 (EL100) polymeric nanoparticles (NP) to tackle limitations of solubility. Bergenin-loaded EL100 nanoparticles (BN-NP) were fabricated via nanoprecipitation and an experimental design was conducted for optimization. A reverse phase-high performance liquid chromatography (RP-HPLC) method was developed for the quantitation of bergenin. The optimized nanoformulation was characterized by its particle size, morphology, loading capacity, entrapment efficiency, drug–excipient interaction and crystallinity. An in vitro assay was executed to gauge the release potential of pH-sensitive nanoformulation. The mean particle size, zeta potential and polydispersity index (PDI) of the optimized nanoparticles were observed to be 86.17 ± 2.1 nm, −32.33 ± 5.53 mV and 0.30 ± 0.03, respectively. The morphological analysis confirmed the spherical nature of the nanoparticles. Drug loading capacity and entrapment efficiency were calculated to be 16 ± 0.34% and 84 ± 1.3%, respectively. Fourier transform infrared spectroscopy (FTIR) studies unfolded that no interaction was present between the drug and the excipients in the nanoformulation. Crystallography studies revealed that the crystalline nature of bergenin was changed to amorphous and the nanoformulation was stable for up to 3 months at 40 °C. The present study confirms that bergenin isolation can be scaled up from abundantly growing B. ciliata. Moreover, it could also be delivered by entrapment in stimuli-responsive polymer, preventing the loss of drug in healthy tissues.
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spelling pubmed-91042312022-05-14 Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata Bashir, Kashaf Khan, Muhammad Farhan Ali Alhodaib, Aiyeshah Ahmed, Naveed Naz, Iffat Mirza, Bushra Tipu, Muhammad Khalid Fatima, Humaira Polymers (Basel) Article The aim of the current study is extraction and isolation of bergenin from Bergenia ciliata and fabrication of pH-sensitive Eudragit(®) L100 (EL100) polymeric nanoparticles (NP) to tackle limitations of solubility. Bergenin-loaded EL100 nanoparticles (BN-NP) were fabricated via nanoprecipitation and an experimental design was conducted for optimization. A reverse phase-high performance liquid chromatography (RP-HPLC) method was developed for the quantitation of bergenin. The optimized nanoformulation was characterized by its particle size, morphology, loading capacity, entrapment efficiency, drug–excipient interaction and crystallinity. An in vitro assay was executed to gauge the release potential of pH-sensitive nanoformulation. The mean particle size, zeta potential and polydispersity index (PDI) of the optimized nanoparticles were observed to be 86.17 ± 2.1 nm, −32.33 ± 5.53 mV and 0.30 ± 0.03, respectively. The morphological analysis confirmed the spherical nature of the nanoparticles. Drug loading capacity and entrapment efficiency were calculated to be 16 ± 0.34% and 84 ± 1.3%, respectively. Fourier transform infrared spectroscopy (FTIR) studies unfolded that no interaction was present between the drug and the excipients in the nanoformulation. Crystallography studies revealed that the crystalline nature of bergenin was changed to amorphous and the nanoformulation was stable for up to 3 months at 40 °C. The present study confirms that bergenin isolation can be scaled up from abundantly growing B. ciliata. Moreover, it could also be delivered by entrapment in stimuli-responsive polymer, preventing the loss of drug in healthy tissues. MDPI 2022-04-19 /pmc/articles/PMC9104231/ /pubmed/35566808 http://dx.doi.org/10.3390/polym14091639 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bashir, Kashaf
Khan, Muhammad Farhan Ali
Alhodaib, Aiyeshah
Ahmed, Naveed
Naz, Iffat
Mirza, Bushra
Tipu, Muhammad Khalid
Fatima, Humaira
Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title_full Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title_fullStr Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title_full_unstemmed Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title_short Design and Evaluation of pH-Sensitive Nanoformulation of Bergenin Isolated from Bergenia ciliata
title_sort design and evaluation of ph-sensitive nanoformulation of bergenin isolated from bergenia ciliata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104231/
https://www.ncbi.nlm.nih.gov/pubmed/35566808
http://dx.doi.org/10.3390/polym14091639
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