Photo-Cross-Linked Biodegradable Poly(Ester Anhydride) Networks Prepared from Alkenylsuccinic Anhydride Functionalized Poly(ε-caprolactone) Precursors

2011 ◽  
Vol 12 (7) ◽  
pp. 2806-2814 ◽  
Author(s):  
Risto A. Hakala ◽  
Harri Korhonen ◽  
Ville V. Meretoja ◽  
Jukka V. Seppälä
2020 ◽  
Vol 62 (6) ◽  
pp. 697-705
Author(s):  
Sarra Benguella ◽  
Aicha Hachemaoui ◽  
Ahmed Yahiaoui ◽  
Abdelkader Dehbi

2021 ◽  
Vol 22 (11) ◽  
pp. 5557
Author(s):  
Tao-Chieh Yang ◽  
Shih-Jung Liu ◽  
Wei-Lun Lo ◽  
Shu-Mei Chen ◽  
Ya-Ling Tang ◽  
...  

Glioblastoma multiforme (GBM) has remained one of the most lethal and challenging cancers to treat. Previous studies have shown encouraging results when irinotecan was used in combination with temozolomide (TMZ) for treating GBM. However, irinotecan has a narrow therapeutic index: a slight dose increase in irinotecan can induce toxicities that outweigh its therapeutic benefits. SN-38 is the active metabolite of irinotecan that accounts for both its anti-tumor efficacy and toxicity. In our previous paper, we showed that SN-38 embedded into 50:50 biodegradable poly[(d,l)-lactide-co-glycolide] (PLGA) microparticles (SMPs) provides an efficient delivery and sustained release of SN-38 from SMPs in the brain tissues of rats. These properties of SMPs give them potential for therapeutic application due to their high efficacy and low toxicity. In this study, we tested the anti-tumor activity of SMP-based interstitial chemotherapy combined with TMZ using TMZ-resistant human glioblastoma cell line-derived xenograft models. Our data suggest that treatment in which SMPs are combined with TMZ reduces tumor growth and extends survival in mice bearing xenograft tumors derived from both TMZ-resistant and TMZ-sensitive human glioblastoma cell lines. Our findings demonstrate that combining SMPs with TMZ may have potential as a promising strategy for the treatment of GBM.


ACS Omega ◽  
2021 ◽  
Author(s):  
Yuki Kawamura ◽  
Hongyi Gan ◽  
Taizo Kabe ◽  
Akira Maehara ◽  
Satoshi Kimura ◽  
...  

2021 ◽  
Author(s):  
Clara Guido ◽  
Mariangela Testini ◽  
Stefania D’Amone ◽  
Barbara Cortese ◽  
Maria Grano ◽  
...  

Capsid-like PGA nanoparticles (NPs) allow sustained cell transfection in 2D and 3D configurations.


Biomedicines ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 682
Author(s):  
Maria Jesus Rodrigo ◽  
David Garcia-Herranz ◽  
Manuel Subias ◽  
Teresa Martinez-Rincón ◽  
Silvia Mendez-Martínez ◽  
...  

 Background: To compare two prolonged animal models of glaucoma over 24 weeks of follow-up. A novel pre-trabecular model of chronic glaucoma was achieved by injection of biodegradable poly lactic-co-glycolic acid (PLGA) microspheres (10–20 µm) (Ms20/10) into the ocular anterior chamber to progressively increase ocular hypertension (OHT). Methods: Rat right eyes were injected to induce OHT: 50% received a suspension of Ms20/10 in the anterior chamber at 0, 2, 4, 8, 12, 16 and 20 weeks, and the other 50% received a sclerosing episcleral vein injection biweekly (EPIm). Ophthalmological clinical signs, intraocular pressure (IOP), neuroretinal functionality measured by electroretinography (ERG), and structural analysis of the retina, retinal nerve fiber layer (RNFL) and ganglion cell layer (GCL) protocols using optical coherence tomography (OCT) and histological exams were performed. Results: Both models showed progressive neuroretinal degeneration (p < 0.05), and contralateral eye affectation. The Ms20/10 model showed a more progressive increase in IOP and better preservation of ocular surface. Although no statistical differences were found between models, the EPIm showed a tendency to produce thicker retinal and thinner GCL thicknesses, slower latency and smaller amplitude as measured using ERG, and more aggressive disturbances in retinal histology. In both models, while the GCL showed the greatest percentage loss of thickness, the RNFL showed the greatest and earliest rate of thickness loss. Conclusions: The intracameral model with biodegradable microspheres resulted more like the conditions observed in humans. It was obtained by a less-aggressive mechanism, which allows for adequate study of the pathology over longer periods. 


2019 ◽  
Vol 297 (5) ◽  
pp. 763-769 ◽  
Author(s):  
Feifei Xin ◽  
Meiyu Sui ◽  
Xisheng Liu ◽  
Cong Zhao ◽  
Yueqin Yu

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