Abstract | OBJECTIVES: METHODS: GO-PAMAM was successfully synthesized by covalent bonding between GO and NH2-terminated PAMAM dendrimer (zero generation). To investigate drug loading performance, QSR was loaded on the surface of GO as well as GO-PAMAM. Further, the release behaviour of QSR-loaded GO-PAMAM was studied. Finally, an in-vitro sulforhodamine B assay was performed in HEK 293T epithelial cells and MDA MB 231 breast cancer cells. KEY FINDINGS: It was observed that GO-PAMAM shows higher QSR loading capacity compared to GO. Also, synthesized nanocarrier exhibits controlled as well as pH-responsive release of QSR and the amount of QSR released at pH 4 was approximately two times higher than the release at pH 7.4. Furthermore, GO-PAMAM was found to be biocompatible for HEK 293T cells, and a high cytotoxic effect was observed for QSR-loaded GO-PAMAM on MDA MB 231 cells. CONCLUSIONS: The present investigation highlights the potential application of synthesized hybrid materials as a nanocarrier with excellent loading and controlled releasing efficiency for the delivery of the hydrophobic anticancer drug.
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Authors | Monika Matiyani, Anita Rana, Mintu Pal, Sumit Dokwal, Nanda Gopal Sahoo |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 75
Issue 6
Pg. 859-872
(Jun 05 2023)
ISSN: 2042-7158 [Electronic] England |
PMID | 37134308
(Publication Type: Journal Article)
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Copyright | © The Author(s) 2023. Published by Oxford University Press on behalf of the Royal Pharmaceutical Society. All rights reserved. For permissions, please e-mail: [email protected]. |
Chemical References |
- Dendrimers
- Poly(amidoamine)
- graphene oxide
- Quercetin
- Antineoplastic Agents
- Drug Carriers
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Topics |
- Humans
- Female
- Dendrimers
(chemistry, pharmacology)
- Breast Neoplasms
(drug therapy)
- Quercetin
(pharmacology)
- Antineoplastic Agents
(pharmacology, chemistry)
- Hydrogen-Ion Concentration
- Drug Carriers
(chemistry)
- Drug Delivery Systems
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