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HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.

The current study was intended to explore the phytochemical profiling and therapeutic activities of Putranjiva roxburghii Wall. Crude extracts of different plant parts were subjected to the determination of antioxidant, antimicrobial, antidiabetic, cytotoxic, and protein kinase inhibitory potential...

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Autores principales: Nazli, Adila, Irshad Khan, Muhammad Zafar, Ahmed, Madiha, Akhtar, Nosheen, Okla, Mohammad K., Al-Hashimi, Abdulrahman, Al-Qahtani, Wahidah H., Abdelgawad, Hamada, Haq, Ihsan-ul-
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746485/
https://www.ncbi.nlm.nih.gov/pubmed/35011299
http://dx.doi.org/10.3390/molecules27010068
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author Nazli, Adila
Irshad Khan, Muhammad Zafar
Ahmed, Madiha
Akhtar, Nosheen
Okla, Mohammad K.
Al-Hashimi, Abdulrahman
Al-Qahtani, Wahidah H.
Abdelgawad, Hamada
Haq, Ihsan-ul-
author_facet Nazli, Adila
Irshad Khan, Muhammad Zafar
Ahmed, Madiha
Akhtar, Nosheen
Okla, Mohammad K.
Al-Hashimi, Abdulrahman
Al-Qahtani, Wahidah H.
Abdelgawad, Hamada
Haq, Ihsan-ul-
author_sort Nazli, Adila
collection PubMed
description The current study was intended to explore the phytochemical profiling and therapeutic activities of Putranjiva roxburghii Wall. Crude extracts of different plant parts were subjected to the determination of antioxidant, antimicrobial, antidiabetic, cytotoxic, and protein kinase inhibitory potential by using solvents of varying polarity ranges. Maximum phenolic content was notified in distilled water extracts of the stem (DW-S) and leaf (DW-L) while the highest flavonoid content was obtained in ethyl acetate leaf (EA-L) extract. HPLC-DAD analysis confirmed the presence of various polyphenols, quantified in the range of 0.02 ± 0.36 to 2.05 ± 0.18 μg/mg extract. Maximum DPPH scavenging activity was expressed by methanolic extract of the stem (MeOH-S). The highest antioxidant capacity and reducing power was shown by MeOH-S and leaf methanolic extract (MeOH-L), respectively. Proficient antibacterial activity was shown by EA-L extract against Bacillus subtilis and Escherichia coli. Remarkable α-amylase and α-glucosidase inhibition potential was expressed by ethyl acetate fruit (EA-F) and n-Hexane leaf (nH-L) extracts, respectively. In case of brine shrimp lethality assay, 41.67% of the extracts (LC(50) < 50 µg/mL) were considered as extremely cytotoxic. The test extracts also showed mild antifungal and protein kinase inhibition activities. The present study explores the therapeutic potential of P. roxburghii and calls for subsequent studies to isolate new bioactive leads through bioactivity-guided isolation.
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spelling pubmed-87464852022-01-11 HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall. Nazli, Adila Irshad Khan, Muhammad Zafar Ahmed, Madiha Akhtar, Nosheen Okla, Mohammad K. Al-Hashimi, Abdulrahman Al-Qahtani, Wahidah H. Abdelgawad, Hamada Haq, Ihsan-ul- Molecules Article The current study was intended to explore the phytochemical profiling and therapeutic activities of Putranjiva roxburghii Wall. Crude extracts of different plant parts were subjected to the determination of antioxidant, antimicrobial, antidiabetic, cytotoxic, and protein kinase inhibitory potential by using solvents of varying polarity ranges. Maximum phenolic content was notified in distilled water extracts of the stem (DW-S) and leaf (DW-L) while the highest flavonoid content was obtained in ethyl acetate leaf (EA-L) extract. HPLC-DAD analysis confirmed the presence of various polyphenols, quantified in the range of 0.02 ± 0.36 to 2.05 ± 0.18 μg/mg extract. Maximum DPPH scavenging activity was expressed by methanolic extract of the stem (MeOH-S). The highest antioxidant capacity and reducing power was shown by MeOH-S and leaf methanolic extract (MeOH-L), respectively. Proficient antibacterial activity was shown by EA-L extract against Bacillus subtilis and Escherichia coli. Remarkable α-amylase and α-glucosidase inhibition potential was expressed by ethyl acetate fruit (EA-F) and n-Hexane leaf (nH-L) extracts, respectively. In case of brine shrimp lethality assay, 41.67% of the extracts (LC(50) < 50 µg/mL) were considered as extremely cytotoxic. The test extracts also showed mild antifungal and protein kinase inhibition activities. The present study explores the therapeutic potential of P. roxburghii and calls for subsequent studies to isolate new bioactive leads through bioactivity-guided isolation. MDPI 2021-12-23 /pmc/articles/PMC8746485/ /pubmed/35011299 http://dx.doi.org/10.3390/molecules27010068 Text en © 2021 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
Nazli, Adila
Irshad Khan, Muhammad Zafar
Ahmed, Madiha
Akhtar, Nosheen
Okla, Mohammad K.
Al-Hashimi, Abdulrahman
Al-Qahtani, Wahidah H.
Abdelgawad, Hamada
Haq, Ihsan-ul-
HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title_full HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title_fullStr HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title_full_unstemmed HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title_short HPLC-DAD Based Polyphenolic Profiling and Evaluation of Pharmacological Attributes of Putranjiva roxburghii Wall.
title_sort hplc-dad based polyphenolic profiling and evaluation of pharmacological attributes of putranjiva roxburghii wall.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746485/
https://www.ncbi.nlm.nih.gov/pubmed/35011299
http://dx.doi.org/10.3390/molecules27010068
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