Delivery of acetogenin-enriched Annona muricata Linn leaf extract by folic acid-conjugated and triphenylphosphonium-conjugated poly(glycerol adipate) nanoparticles to enhance toxicity against ovarian cancer cells
dc.contributor.author | Damrongrak K. | |
dc.contributor.author | Kloysawat K. | |
dc.contributor.author | Bunsupa S. | |
dc.contributor.author | Sakchasri K. | |
dc.contributor.author | Wongrakpanich A. | |
dc.contributor.author | Taresco V. | |
dc.contributor.author | Cuzzucoli Crucitti V. | |
dc.contributor.author | Garnett M.C. | |
dc.contributor.author | Suksiriworapong J. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-06-18T18:13:46Z | |
dc.date.available | 2023-06-18T18:13:46Z | |
dc.date.issued | 2022-04-25 | |
dc.description.abstract | The study demonstrated the fabrication of new poly(glycerol adipate) (PGA) nanoparticles decorated with folic acid (FOL-PGA) and triphenylphosphonium (TPP-PGA) and the potential on the delivery of acetogenin-enriched Annona muricata Linn leaf extract to ovarian cancer cells. FOL-PGA and TPP-PGA were successfully synthesized and used to fabricate FOL-decorated nanoparticles (FOL-NPs) and FOL-/TPP- decorated nanoparticles (FOL/TPP-NPs) by blending two polymers at a mass ratio of 1:1. All nanoparticles had small size of around 100 nm, narrow size distribution and high negative surface charge about −30 mV. The stable FOL/TPP-NPs showed highest drug loading of 14.9 ± 1.9% at 1:5 ratio of extract to polymer and reached to 35.8 ± 2.1% at higher ratio. Both nanoparticles released the extract in a biphasic sustained release manner over 5 days. The toxicity of the extract to SKOV3 cells was potentiated by FOL-NPs and FOL/TPP-NPs by 2.0 – 2.6 fold through induction of cell apoptosis. FOL/TPP-NPs showed lower IC50 and higher cellular uptake as compared to FOL-NPs. FOL-NPs exhibited folate receptor-mediated endocytosis. FOL/TPP-NPs provided more advantages than FOL-NPs in terms of stability in physiological fluid, uptake efficiency and targeting ability to mitochondria and showed a promising potential PGA platform for targeted delivery of herbal cytotoxic extracts. | |
dc.identifier.citation | International Journal of Pharmaceutics Vol.618 (2022) | |
dc.identifier.doi | 10.1016/j.ijpharm.2022.121636 | |
dc.identifier.eissn | 18733476 | |
dc.identifier.issn | 03785173 | |
dc.identifier.pmid | 35259439 | |
dc.identifier.scopus | 2-s2.0-85126057180 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/86870 | |
dc.rights.holder | SCOPUS | |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | |
dc.title | Delivery of acetogenin-enriched Annona muricata Linn leaf extract by folic acid-conjugated and triphenylphosphonium-conjugated poly(glycerol adipate) nanoparticles to enhance toxicity against ovarian cancer cells | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85126057180&origin=inward | |
oaire.citation.title | International Journal of Pharmaceutics | |
oaire.citation.volume | 618 | |
oairecerif.author.affiliation | University of Nottingham | |
oairecerif.author.affiliation | Mahidol University |