Development of Berberine-Loaded Nanoparticles for Astrocytoma Cells Administration and Photodynamic Therapy Stimulation
Berberine (BBR) is known for its antitumor activity and photosensitizer properties in anti-cancer photodynamic therapy (PDT), and it has previously been favorably assayed against glioblastoma multiforme (GBM)-derived cells. In this work, two BBR hydrophobic salts, dodecyl sulfate (S) and laurate (L)...
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2023-03-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_af9b8195f7f7403f976d8c5de6711f8f | ||
042 | |a dc | ||
100 | 1 | 0 | |a Sergio Comincini |e author |
700 | 1 | 0 | |a Federico Manai |e author |
700 | 1 | 0 | |a Milena Sorrenti |e author |
700 | 1 | 0 | |a Sara Perteghella |e author |
700 | 1 | 0 | |a Camilla D'Amato |e author |
700 | 1 | 0 | |a Dalila Miele |e author |
700 | 1 | 0 | |a Laura Catenacci |e author |
700 | 1 | 0 | |a Maria Cristina Bonferoni |e author |
245 | 0 | 0 | |a Development of Berberine-Loaded Nanoparticles for Astrocytoma Cells Administration and Photodynamic Therapy Stimulation |
260 | |b MDPI AG, |c 2023-03-01T00:00:00Z. | ||
500 | |a 10.3390/pharmaceutics15041078 | ||
500 | |a 1999-4923 | ||
520 | |a Berberine (BBR) is known for its antitumor activity and photosensitizer properties in anti-cancer photodynamic therapy (PDT), and it has previously been favorably assayed against glioblastoma multiforme (GBM)-derived cells. In this work, two BBR hydrophobic salts, dodecyl sulfate (S) and laurate (L), have been encapsulated in PLGA-based nanoparticles (NPs), chitosan-coated by the addition of chitosan oleate in the preparation. NPs were also further functionalized with folic acid. All the BBR-loaded NPs were efficiently internalized into T98G GBM established cells, and internalization increased in the presence of folic acid. However, the highest mitochondrial co-localization percentages were obtained with BBR-S NPs without folic acid content. In the T98G cells, BBR-S NPs appeared to be the most efficient in inducing cytotoxicity events and were therefore selected to assess the effect of photodynamic stimulation (PDT). As a result, PDT potentiated the viability reduction for the BBR-S NPs at all the studied concentrations, and a roughly 50% reduction of viability was obtained. No significant cytotoxic effect on normal rat primary astrocytes was observed. In GBM cells, a significant increase in early and late apoptotic events was scored by BBR NPs, with a further increase following the PDT scheme. Furthermore, a significantly increased depolarization of mitochondria was highlighted following BBR-S NPs' internalization and mostly after PDT stimulation, compared to untreated and PDT-only treated cells. In conclusion, these results highlighted the efficacy of the BBR-NPs-based strategy coupled with photoactivation approaches to induce favorable cytotoxic effects in GBM cells. | ||
546 | |a EN | ||
690 | |a PLGA-nanoparticles | ||
690 | |a glioblastoma | ||
690 | |a cancer | ||
690 | |a chitosan oleate | ||
690 | |a berberine | ||
690 | |a hydrophobic salts | ||
690 | |a Pharmacy and materia medica | ||
690 | |a RS1-441 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Pharmaceutics, Vol 15, Iss 4, p 1078 (2023) | |
787 | 0 | |n https://www.mdpi.com/1999-4923/15/4/1078 | |
787 | 0 | |n https://doaj.org/toc/1999-4923 | |
856 | 4 | 1 | |u https://doaj.org/article/af9b8195f7f7403f976d8c5de6711f8f |z Connect to this object online. |