Journal of Pharmaceutical Innovation, Journal Year: 2024, Volume and Issue: 19(6)
Published: Dec. 1, 2024
Language: Английский
Journal of Pharmaceutical Innovation, Journal Year: 2024, Volume and Issue: 19(6)
Published: Dec. 1, 2024
Language: Английский
Drug Development and Industrial Pharmacy, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 12
Published: Jan. 16, 2025
The objective of the study was to tackle recurrence prostate cancer (PCa) post-surgery and re-sensitize docetaxel (DTX)-resistant PC-3 cells chemo-therapy using NIC. Prolonged DTX therapy leads emergence chemo-resistance by overexpression PI3K-AKT pathway in PCa along with tumor post-surgery. Suppression this could be essential improving anticancer activity re-sensitizing resistant cells. Niclosamide (NIC), an anthelmintic drug has shown tremendous potential re-sensitized various drugs. To mitigate post-surgical recurrence, implant-based system facilitating sustained release NIC beneficial. were incorporated within a nanofiber (NF) prevent on-site local DTX-resistant fabricated DTX-NIC NF via electrospinning 334 ± 96.14 nm diameter demonstrated profile till 6 d. Elevated mitochondrial damage, reactive oxygen species levels apoptotic index revealed improvement cytotoxicity post incorporation into owing their profile. Re-sensitization PC-3/DTX observed introduction which due suppression p-Akt1, overexpressed From superior re-sensitization cells, we conclude that beneficial therapeutic regimen preventing PCa.
Language: Английский
Citations
7BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)
Published: Feb. 5, 2025
Language: Английский
Citations
6Journal of drug targeting, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 21
Published: Jan. 20, 2025
The purpose of this work was to create and assess Lornoxicam (LOR) loaded Novasomes (Novas) for the efficient treatment ulcerative colitis. study performed using a 23 factorial design investigate impact several formulation variables. Three separate parameters were investigated: Surface Active agent (SAA) type (X1), LOR concentration (X2), SAA: Oleic acid ratio (X3). dependent responses included encapsulation efficiency (Y1: EE %), particle size (Y2: PS), zeta potential (Y3: ZP), polydispersity index (Y4: PDI). vesicles demonstrated remarkable efficiency, ranging from 81.32 ± 3.24 98.64 0.99%. vesicle sizes ranged 329 9.88 583.4 9.04 nm with high negative values. release pattern Novas' biphasic adhered Higuchi's model. An in-vivo assessed how LOR-Novas affected rats' acetic acid-induced colitis (UC). optimized effectively reduced colonic ulceration (P < 0.05) inflammatory pathway via inhibiting Toll-like receptor 4 (TLR4), Nuclear factor kappa β (NF-κβ) inducible nitric oxide (iNO). At same time, it elevated Silent information regulator-1(SIRT-1) glutathione (GSH) colon contents. Thus, current suggested that LOR- Novas may be viable
Language: Английский
Citations
2Journal of Liposome Research, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 15
Published: Feb. 2, 2025
Personalized treatment strategies have greatly improved the efficacy of anticancer drugs. Nanocarriers, especially liposomes, function as excellent platform for delivery both hydrophilic and hydrophobic agents. iRGD is a peptide composed 9-amino acid denoted (iRGDP), enhances selective intratumoral Trastuzumab (TMAB), mainly targets HER2-positive advanced stage breast cancer an FDA-approved monoclonal antibody. Gefitinib (GEB) drug, effective against metastatic (MBC), while Lycorine hydrochloride (LCOH), naturally derived compound, possess anti-inflammatory properties. This research emphasizing on preparation GEB LCOH-entrapped TPGS-COOH coated-liposomes, camouflaged with antibody (TMAB) cyclic (iRGDP) targeted in MBC therapy. The developed multifunctional liposomes were studied extensive vitro cell line studies MCF-7 cells. half-maximum inhibitory concentration (IC-50) values LCOH co-loaded single functionalized liposome (SFL) (iRGDP-LiP, TMAB-LiP) dual-functionalized (DFL) (iRGDP-TMAB-LiP) cells 1.04 ± 0.023 μg/mL, 0.71 0.018 0.56 0.028 respectively. Inverted confocal laser scanning microscopy (ICLSM) revealed enhanced cellular internalization SFL DFL-treated groups tagged coumarin-6 rhodamine-B dye compared to conventional liposome. scratch assay marked reduction migration, DAPI staining confirmed nuclear condensation (NC) fragmentation (NF) groups. Moreover, flow cytometry demonstrated early late apoptosis DFL These findings indicate that holds promise multifaceted therapeutic approach
Language: Английский
Citations
2Journal of Controlled Release, Journal Year: 2024, Volume and Issue: 368, P. 703 - 727
Published: March 19, 2024
Drug delivery platforms have gracefully emerged as an indispensable component of novel cancer chemotherapy, bestowing targeted drug distribution, elevating therapeutic effects, and reducing the burden unwanted side effects. In this context, hybrid systems artfully harnessing virtues liposomes hydrogels bring remarkable benefits, especially for localized therapy, including intensified stability, excellent amenability to hydrophobic hydrophilic medications, controlled liberation behavior, appropriate mucoadhesion mucopenetration shift. Moreover, three-dimensional biocompatible liposome-integrated hydrogel networks attracted unprecedented interest in tissue regeneration, given their tunable architecture physicochemical properties, well enhanced mechanical support. This review elucidates presents cutting-edge developments recruiting treatment regeneration.
Language: Английский
Citations
15European Journal of Pharmaceutics and Biopharmaceutics, Journal Year: 2023, Volume and Issue: 190, P. 94 - 106
Published: July 18, 2023
Language: Английский
Citations
18Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 99, P. 105977 - 105977
Published: July 14, 2024
Language: Английский
Citations
8Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 92, P. 105399 - 105399
Published: Jan. 21, 2024
Language: Английский
Citations
5Brain Research, Journal Year: 2024, Volume and Issue: unknown, P. 149411 - 149411
Published: Dec. 1, 2024
Language: Английский
Citations
5Colloids and Surfaces B Biointerfaces, Journal Year: 2023, Volume and Issue: 234, P. 113732 - 113732
Published: Dec. 27, 2023
Language: Английский
Citations
11