Antiproliferative and Apoptotic Effects of pH‐Responsive Veratric Acid‐Loaded Polydopamine Nanoparticles in Human Triple Negative Breast Cancer Cells

Veratric acid (VA) is plant‐derived phenolic acid known for its therapeutic potential, but its anticancer effect on highly invasive triple‐negative breast cancer (TNBC) is yet to be evaluated. Polydopamine nanoparticles (nPDAs) were chosen as the drug carrier to overcome VA's hydrophobic nature...

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Veröffentlicht in:Chemistry & biodiversity 2023-06, Vol.20 (6), p.e202201006-n/a
Hauptverfasser: Harini, Ganesh, Shree Ganesh, S., Anushikaa, Ramprasad, Bharathi, Ramanathan, Aravind, Sankaranarayanan, Vatsala, Kumari, Shanmugavadivu, Abinaya, Selvamurugan, Nagarajan
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container_issue 6
container_start_page e202201006
container_title Chemistry & biodiversity
container_volume 20
creator Harini, Ganesh
Shree Ganesh, S.
Anushikaa, Ramprasad
Bharathi, Ramanathan
Aravind, Sankaranarayanan
Vatsala, Kumari
Shanmugavadivu, Abinaya
Selvamurugan, Nagarajan
description Veratric acid (VA) is plant‐derived phenolic acid known for its therapeutic potential, but its anticancer effect on highly invasive triple‐negative breast cancer (TNBC) is yet to be evaluated. Polydopamine nanoparticles (nPDAs) were chosen as the drug carrier to overcome VA's hydrophobic nature and ensure a sustained release of VA. We prepared pH‐sensitive nano‐formulations of VA‐loaded nPDAs and subjected them to physicochemical characterization and in vitro drug release studies, followed by cell viability and apoptotic assays on TNBC cells (MDA‐MB‐231 cells). The SEM and zeta analysis revealed spherical nPDAs were uniform size distribution and good colloidal stability. In vitro drug release from VA‐nPDAs was sustained, prolonged and pH‐sensitive, which could benefit tumor cell targeting. MTT and cell viability assays showed that VA‐nPDAs (IC50=17.6 μM) are more antiproliferative towards MDA‐MB‐231 cells than free VA (IC50=437.89 μM). The induction of early and late apoptosis by VA‐nPDAs in the cancer cells was identified using annexin V and dead cell assay. Thus, the pH response and sustained release of VA from nPDAs showed the potential to enter the cell, inhibit cell proliferation, and induce apoptosis in human breast cancer cells, indicating the anticancer potential of VA.
doi_str_mv 10.1002/cbdv.202201006
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Polydopamine nanoparticles (nPDAs) were chosen as the drug carrier to overcome VA's hydrophobic nature and ensure a sustained release of VA. We prepared pH‐sensitive nano‐formulations of VA‐loaded nPDAs and subjected them to physicochemical characterization and in vitro drug release studies, followed by cell viability and apoptotic assays on TNBC cells (MDA‐MB‐231 cells). The SEM and zeta analysis revealed spherical nPDAs were uniform size distribution and good colloidal stability. In vitro drug release from VA‐nPDAs was sustained, prolonged and pH‐sensitive, which could benefit tumor cell targeting. MTT and cell viability assays showed that VA‐nPDAs (IC50=17.6 μM) are more antiproliferative towards MDA‐MB‐231 cells than free VA (IC50=437.89 μM). The induction of early and late apoptosis by VA‐nPDAs in the cancer cells was identified using annexin V and dead cell assay. 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Thus, the pH response and sustained release of VA from nPDAs showed the potential to enter the cell, inhibit cell proliferation, and induce apoptosis in human breast cancer cells, indicating the anticancer potential of VA.</description><subject>Annexin V</subject><subject>Anticancer properties</subject><subject>antiproliferative</subject><subject>Antiproliferatives</subject><subject>Apoptosis</subject><subject>Assaying</subject><subject>Breast cancer</subject><subject>Cell proliferation</subject><subject>Cell viability</subject><subject>Controlled release</subject><subject>Drug carriers</subject><subject>Drug delivery</subject><subject>Hydrophobicity</subject><subject>Nanoparticles</subject><subject>pH effects</subject><subject>Phenolic acids</subject><subject>Phenols</subject><subject>polydopamine nanoparticles</subject><subject>Size distribution</subject><subject>Sustained release</subject><subject>triple negative breast cancer</subject><subject>veratric acid</subject><issn>1612-1872</issn><issn>1612-1880</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkc9u1DAQxiMEon_gyhFZ4sJlF9tJHOe4TVsWaQUIlV6jiT1GrhI72EnR3ngErrweT4KjLYvEhdPMeH7zzchflr1gdM0o5W9Up-_XnHJOUykeZadMML5iUtLHx7ziJ9lZjHeJT-_yaXaSV6ygdSVOs58bN9kx-N4aDDDZeyTgNNmMfpz8ZBW5MgbVFIk3ZNz--v7jE8bRu7iAt8tESMxGWZ1aOw8aNfno-732IwzWIXkPLqUhKfUYiXVkOw_gyE2wY5-6-OWw8yIgxIk04BQG0mDfx2fZEwN9xOcP8Tz7fH1102xXuw9v3zWb3UrlVS5WXVkVnSk5lnUuUEuta6RYdKCNZNoAgJAISnCpGadasAqA8Ro7nlNZViw_z14fdNMvfJ0xTu1go0oXgEM_x5ZLWpdFUeQioa_-Qe_8HFy6LlFc5lVRioVaHygVfIwBTTsGO0DYt4y2i2ntYlp7NC0NvHyQnbsB9RH_41IC6gPwzfa4_49c21xc3v4V_w19A6ej</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Harini, Ganesh</creator><creator>Shree Ganesh, S.</creator><creator>Anushikaa, Ramprasad</creator><creator>Bharathi, Ramanathan</creator><creator>Aravind, Sankaranarayanan</creator><creator>Vatsala, Kumari</creator><creator>Shanmugavadivu, Abinaya</creator><creator>Selvamurugan, Nagarajan</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3713-1920</orcidid></search><sort><creationdate>202306</creationdate><title>Antiproliferative and Apoptotic Effects of pH‐Responsive Veratric Acid‐Loaded Polydopamine Nanoparticles in Human Triple Negative Breast Cancer Cells</title><author>Harini, Ganesh ; Shree Ganesh, S. ; Anushikaa, Ramprasad ; Bharathi, Ramanathan ; Aravind, Sankaranarayanan ; Vatsala, Kumari ; Shanmugavadivu, Abinaya ; Selvamurugan, Nagarajan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3736-b574bf52e5936ed8dd9e0e4badf81dfaaa68eac628d120d617aa129eb23085713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Annexin V</topic><topic>Anticancer properties</topic><topic>antiproliferative</topic><topic>Antiproliferatives</topic><topic>Apoptosis</topic><topic>Assaying</topic><topic>Breast cancer</topic><topic>Cell proliferation</topic><topic>Cell viability</topic><topic>Controlled release</topic><topic>Drug carriers</topic><topic>Drug delivery</topic><topic>Hydrophobicity</topic><topic>Nanoparticles</topic><topic>pH effects</topic><topic>Phenolic acids</topic><topic>Phenols</topic><topic>polydopamine nanoparticles</topic><topic>Size distribution</topic><topic>Sustained release</topic><topic>triple negative breast cancer</topic><topic>veratric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harini, Ganesh</creatorcontrib><creatorcontrib>Shree Ganesh, S.</creatorcontrib><creatorcontrib>Anushikaa, Ramprasad</creatorcontrib><creatorcontrib>Bharathi, Ramanathan</creatorcontrib><creatorcontrib>Aravind, Sankaranarayanan</creatorcontrib><creatorcontrib>Vatsala, Kumari</creatorcontrib><creatorcontrib>Shanmugavadivu, Abinaya</creatorcontrib><creatorcontrib>Selvamurugan, Nagarajan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; 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source Wiley-Blackwell Journals
subjects Annexin V
Anticancer properties
antiproliferative
Antiproliferatives
Apoptosis
Assaying
Breast cancer
Cell proliferation
Cell viability
Controlled release
Drug carriers
Drug delivery
Hydrophobicity
Nanoparticles
pH effects
Phenolic acids
Phenols
polydopamine nanoparticles
Size distribution
Sustained release
triple negative breast cancer
veratric acid
title Antiproliferative and Apoptotic Effects of pH‐Responsive Veratric Acid‐Loaded Polydopamine Nanoparticles in Human Triple Negative Breast Cancer Cells
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