Journal of Molecular Liquids, Journal Year: 2024, Volume and Issue: unknown, P. 126541 - 126541
Published: Nov. 1, 2024
Language: Английский
Journal of Molecular Liquids, Journal Year: 2024, Volume and Issue: unknown, P. 126541 - 126541
Published: Nov. 1, 2024
Language: Английский
Colloids and Surfaces A Physicochemical and Engineering Aspects, Journal Year: 2024, Volume and Issue: 698, P. 134587 - 134587
Published: Oct. 1, 2024
Language: Английский
Citations
8Drug Delivery and Translational Research, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 10, 2025
Language: Английский
Citations
1Wear, Journal Year: 2025, Volume and Issue: unknown, P. 205931 - 205931
Published: Feb. 1, 2025
Language: Английский
Citations
1Nano Energy, Journal Year: 2023, Volume and Issue: 119, P. 109080 - 109080
Published: Nov. 11, 2023
Language: Английский
Citations
19Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(4), P. 437 - 437
Published: March 22, 2024
The production of tailored, on-demand drug delivery systems has gained attention in pharmaceutical development over the last few years, thanks to application 3D printing technology field. Recently, direct powder extrusion (DPE) emerged among extrusion-based additive manufacturing techniques. It is a one-step procedure that allows processing powdered formulations. aim this systematic literature review analyze using DPE. A total 27 articles have been identified through scientific databases (Scopus, PubMed, and ScienceDirect). main characteristics three types printers based on DPE discussed. selection polymers auxiliary excipients, as well flowability mixture, rheological properties molten material, temperatures critical parameters for successful printing. wide range with varied geometries different release profiles intended oral, buccal, parenteral, transdermal routes produced. ability technique manufacture personalized, proven. For all these reasons, its implementation hospital settings near future seems promising.
Language: Английский
Citations
6Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 99, P. 105973 - 105973
Published: July 16, 2024
To overcome the challenges of blood-brain barrier for drug delivery to central nervous system (CNS), intranasal implants were developed improve management CNS conditions, such as schizophrenia. In present work, we and characterised a drug-containing implant consisting two parts: core layer made from risperidone (RIS) water-soluble polymers, including poly(vinylpyrrolidone) (PVP) poly(ethylene glycol) (PEG), coating poly(caprolactone) (PCL) membrane. The obtained implants, where contained 75 % w/w risperidone, using several techniques: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), differential calorimetry (DSC), attenuated total reflectance-Fourier transform infrared (ATR-FTIR). Moreover, in vitro release profile RIS was studied, showing that PCL membrane could extend 2 days up 100 days. PCL-coated exhibited linear over first 10 days, followed by slower rate reached another phase 40 Subsequently, rates progressively slowed down. Finally, results biocompatibility studies indicated biocompatible non-cytotoxic. These findings suggest prepared this work have potential provide long-acting targeting brain.
Language: Английский
Citations
6Acta Biomaterialia, Journal Year: 2024, Volume and Issue: 185, P. 203 - 214
Published: July 23, 2024
Language: Английский
Citations
6iScience, Journal Year: 2024, Volume and Issue: 27(11), P. 111185 - 111185
Published: Oct. 17, 2024
Language: Английский
Citations
6Drug Delivery and Translational Research, Journal Year: 2023, Volume and Issue: 14(1), P. 208 - 222
Published: July 21, 2023
Research on the use of microarray patches (MAPs) has progressed at an unprecedented rate over years, leading to development many novel drug delivery systems. As technology approaches patients, there are several key aspects that ought be addressed in order facilitate smooth translation MAPs from bench bedside. One integral factor includes choice devices and packaging for storage MAPs. In current work, a slide-and-seal box, MAP-box, was developed dissolving MAPs, using fused-deposition modelling. The device been designed act as pill-box not only provide protection environment, but also improve patient's adherence treatment. overall design MAP-box simple, yet offers capability sealing protecting up 30 days. Donepezil HCl formulated into dissolvable MAP, which used treat dementia related Alzheimer's disease. This compound model formulation evaluate utility 3D printed when placed under three conditions: 5 °C ambient humidity, 25 65% relative humidity 40 75% humidity. It shown box able confer days accelerated stability study conditions loading, mechanical properties insertion remained unaffected compared unpackaged stored these same parameters. These preliminary data evidence prototype may great single or multiple Nevertheless, future work will needed their patient usability its application different types MAP systems fully validate robustness prototype.
Language: Английский
Citations
14Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)
Published: Jan. 2, 2024
Abstract Triple-negative breast cancer (TNBC) treatment is challenging and frequently characterized by an aggressive phenotype low prognosis in comparison to other subtypes. This paper presents fabricated implantable drug-loaded microporous poly-di-methyl-siloxane (PDMS) devices for the delivery of targeted therapeutic agents [Luteinizing Hormone-Releasing Hormone conjugated paclitaxel (PTX-LHRH) Luteinizing prodigiosin (PG-LHRH)] possible prevention triple-negative recurrence. In vitro assessment using Alamar blue assay demonstrated a significant reduction (p < 0.05) percentage cell growth time-dependent manner groups treated with PG, PG-LHRH, PTX, PTX-LHRH. Subcutaneous xenograft tumors were then induced athymic female nude mice that four weeks old. Two later, surgically but partially removed, device implanted. Mice observed tumor regrowth organ toxicity. The animal study revealed there was no regrowth, six post-treatment, when LHRH drugs (LHRH-PTX LHRH-PGS) used treatment. cytotoxic effects released on liver, kidney, lung are assessed quantitative biochemical from blood samples groups. Ex vivo histopathological results tissues showed did not induce any adverse effect kidneys, or lungs, based qualitative toxicity studies. implications discussed localized triple negative cancer.
Language: Английский
Citations
5