Co-delivery of paclitaxel and etoposide prodrug by human serum albumin and PLGA nanoparticles : synergistic cytotoxicity in brain tumour cells
The aims of this study were to develop co-delivery systems of paclitaxel (PTX) and etoposide prodrug (4'-O-benzyloxycarbonyl-etoposide, ETP-cbz) based on non-cross-linked human serum albumin (HSA) and poly(lactide-co-glycolide) nanoparticles and to evaluate the synergistic potential of these drugs in vitro. The nanoformulations were prepared by the high-pressure homogenisation technique and characterised using DLS, TEM, SEM, AFM, HPLC, CZE, in-vitro release, and cytotoxicity in human and murine glioma cells. All nanoparticles had 90-150 nm in size and negative ζ-potentials. The Neuro2A cells were the most sensitive to both HSA- and PLGA-based co-delivery systems (IC50 0.024 µM and 0.053 µM, respectively). The drugs' synergistic effect (combination index < 0.9) was observed in the GL261 cells for both types of co-delivery formulations and in the Neuro2A cells for the HSA-based system. These nanodelivery systems may be useful to improve combination chemotherapy for brain tumour treatment. To our knowledge, this is the first report describing the non-cross-linked HSA-based co-delivery nanosuspension which was prepared using nab™ technology.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:40 |
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Enthalten in: |
Journal of microencapsulation - 40(2023), 4 vom: 16. Juni, Seite 246-262 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Kovshova, Tatyana [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 15.05.2023 Date Revised 15.05.2023 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1080/02652048.2023.2188943 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM353862789 |
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520 | |a The aims of this study were to develop co-delivery systems of paclitaxel (PTX) and etoposide prodrug (4'-O-benzyloxycarbonyl-etoposide, ETP-cbz) based on non-cross-linked human serum albumin (HSA) and poly(lactide-co-glycolide) nanoparticles and to evaluate the synergistic potential of these drugs in vitro. The nanoformulations were prepared by the high-pressure homogenisation technique and characterised using DLS, TEM, SEM, AFM, HPLC, CZE, in-vitro release, and cytotoxicity in human and murine glioma cells. All nanoparticles had 90-150 nm in size and negative ζ-potentials. The Neuro2A cells were the most sensitive to both HSA- and PLGA-based co-delivery systems (IC50 0.024 µM and 0.053 µM, respectively). The drugs' synergistic effect (combination index < 0.9) was observed in the GL261 cells for both types of co-delivery formulations and in the Neuro2A cells for the HSA-based system. These nanodelivery systems may be useful to improve combination chemotherapy for brain tumour treatment. To our knowledge, this is the first report describing the non-cross-linked HSA-based co-delivery nanosuspension which was prepared using nab™ technology | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Co-delivery | |
650 | 4 | |a GL261 glioma cells | |
650 | 4 | |a HSA nanoparticles | |
650 | 4 | |a Neuro-2a neuroblastoma cells | |
650 | 4 | |a PLGA nanoparticles | |
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650 | 4 | |a paclitaxel | |
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700 | 1 | |a Mantrov, Sergey |e verfasserin |4 aut | |
700 | 1 | |a Boiko, Svetlana |e verfasserin |4 aut | |
700 | 1 | |a Malinovskaya, Julia |e verfasserin |4 aut | |
700 | 1 | |a Merkulova, Maria |e verfasserin |4 aut | |
700 | 1 | |a Osipova, Nadezhda |e verfasserin |4 aut | |
700 | 1 | |a Moiseeva, Natalia |e verfasserin |4 aut | |
700 | 1 | |a Akimov, Mikhail |e verfasserin |4 aut | |
700 | 1 | |a Dudina, Polina |e verfasserin |4 aut | |
700 | 1 | |a Senchikhin, Ivan |e verfasserin |4 aut | |
700 | 1 | |a Ermolenko, Yulia |e verfasserin |4 aut | |
700 | 1 | |a Gelperina, Svetlana |e verfasserin |4 aut | |
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