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Preparation and Evaluation of Diosmin-Loaded Diphenylcarbonate-Cross-Linked Cyclodextrin Nanosponges for Breast Cancer Therapy
by
Anwer, Md. Khalid
, Iqbal, Muzaffar
, Ahmed, Mohammed Muqtader
, Aldawsari, Mohammed F.
, Kumar, Vinay
in
Antioxidants
/ Apoptosis
/ Bioavailability
/ Breast cancer
/ Cancer therapies
/ caspase
/ Chemotherapy
/ Cytotoxicity
/ Drug delivery systems
/ drug release
/ Hydrogen bonds
/ morphology
/ Particle size
/ phase solubility
/ release kinetics
/ Spectrum analysis
2022
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Preparation and Evaluation of Diosmin-Loaded Diphenylcarbonate-Cross-Linked Cyclodextrin Nanosponges for Breast Cancer Therapy
by
Anwer, Md. Khalid
, Iqbal, Muzaffar
, Ahmed, Mohammed Muqtader
, Aldawsari, Mohammed F.
, Kumar, Vinay
in
Antioxidants
/ Apoptosis
/ Bioavailability
/ Breast cancer
/ Cancer therapies
/ caspase
/ Chemotherapy
/ Cytotoxicity
/ Drug delivery systems
/ drug release
/ Hydrogen bonds
/ morphology
/ Particle size
/ phase solubility
/ release kinetics
/ Spectrum analysis
2022
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Preparation and Evaluation of Diosmin-Loaded Diphenylcarbonate-Cross-Linked Cyclodextrin Nanosponges for Breast Cancer Therapy
by
Anwer, Md. Khalid
, Iqbal, Muzaffar
, Ahmed, Mohammed Muqtader
, Aldawsari, Mohammed F.
, Kumar, Vinay
in
Antioxidants
/ Apoptosis
/ Bioavailability
/ Breast cancer
/ Cancer therapies
/ caspase
/ Chemotherapy
/ Cytotoxicity
/ Drug delivery systems
/ drug release
/ Hydrogen bonds
/ morphology
/ Particle size
/ phase solubility
/ release kinetics
/ Spectrum analysis
2022
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Preparation and Evaluation of Diosmin-Loaded Diphenylcarbonate-Cross-Linked Cyclodextrin Nanosponges for Breast Cancer Therapy
Journal Article
Preparation and Evaluation of Diosmin-Loaded Diphenylcarbonate-Cross-Linked Cyclodextrin Nanosponges for Breast Cancer Therapy
2022
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Overview
In the current study, diosmin (DSM)-loaded beta-cyclodextrin (β-CD)-based nanosponges (NSPs) using diphenylcarbonate (DPC) as a cross-linker were prepared. Four different DSM-loaded NSPs (D-NSP1-NSP4) were developed by varying the molar ratio of β-CD: DCP (1:15–1:6). Based on preliminary evaluations, NSPs (D-NSP3) were optimized for size (412 ± 6.1 nm), polydispersity index (PDI) (0.259), zeta potential (ZP) (−10.8 ± 4.3 mV), and drug loading (DL) (88.7 ± 8.5%), and were further evaluated by in vitro release, scanning electron microscopy (SEM), and in vitro antioxidant studies. The NSPs (D-NSP3) exhibited improved free radical scavenging activity (85.58% at 100 g/mL) compared to pure DSM. Dissolution efficiency (%DE) was enhanced to 71.50% (D-NSP3) from plain DSM (58.59%). The D-NSP3 formulation followed the Korsmeyer–Peppas kinetic model and had an n value of 0.529 indicating a non-Fickian and controlled release by diffusion and relaxation. The D-NSP3 showed cytotoxic activity against MCF-7 breast cancer, as evidenced by caspase 3, 9, and p53 activities. According to the findings, DSM-loaded NSPs might be a promising therapy option for breast cancer.
Publisher
MDPI AG,MDPI
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