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Extracellular vesicles (exosomes) are being continuously investigated by researchers as alternative diagnostic and targeted drug delivery nanocarriers for cancer theranostics. Exosomes are nano-extracellular vesicles that contain different biomolecules, including proteins, lipids, and nucleic acids. The natural intercellular communication tendency in recent discoveries to exhibit distinct characteristics in diseased states makes them more interesting for researchers. The molecular composition of exosomes reflects parent cells or their origin and distinguishes the expression of biomarkers. To improve the efficiency of drug-delivery vesicles, the surface of exosomes can be modified using a variety of stimuli-responsive components, including polymers, targeting ligands, enzymes, etc. Cancer physiological and related drug delivery trends in exosomes can challenge the hurdles associated with the cancer microenvironment. The genetic expression of ligands on exosome surfaces adds unique characteristics to tackle the hurdles of the nonexpressive enhanced permeability and retention (EPR) effect in cancers. This Review covers the structural framework, biogenesis, and explored investigational research on exosomes as a theranostic approach in different cancers. The special emphasis on targeted drug delivery and the multistimuli-responsive potential of exosomes in different cancers are discussed briefly, along with recent achievements in the field, such as patents and clinical trials, for further strengthening this platform and developing more effective exosome-based drug delivery systems for cancer management.
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http://dx.doi.org/10.1021/acsabm.5c00955 | DOI Listing |
N Engl J Med
September 2025
Department of Health Promotion and Policy, School of Public Health and Health Sciences, University of Massachusetts Amherst, Amherst.
Background: In 2019, seven county correctional facilities (jails) in Massachusetts initiated pilot programs to provide all Food and Drug Administration-approved medications for opioid use disorder (MOUD).
Methods: This observational study used linked state data to examine postrelease MOUD receipt, overdose, death, and reincarceration among persons with probable opioid use disorder (OUD) in carceral settings who did or did not receive MOUD from these programs from September 1, 2019, through December 31, 2020. Log-binomial and proportional-hazards models were adjusted for propensity-score weights and baseline covariates that remained imbalanced after propensity-score weighting.
J Med Chem
September 2025
State Key Laboratory of Advanced Drug Delivery and Release Systems, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Resistance-conferring mutations in the androgen receptor (AR) ligand-binding pocket (LBP) compromise the effectiveness of clinically approved orthosteric AR antagonists. Targeting the dimerization interface pocket (DIP) of AR presents a promising therapeutic approach. In this study, we report the design and optimization of -(thiazol-2-yl) furanamide derivatives as novel AR DIP antagonists, among which was the most promising candidate.
View Article and Find Full Text PDFEpidemiol Serv Saude
September 2025
Universidade de Brasília, Faculdade de Ciências e Tecnologias em Saúde, Brasília, DF, Brazil.
Objective: Systematize the methodological decisions adopted in the budget impact analyses of the recommendation reports of the National Commission for the Incorporation of Technologies into the Unified Health System (Conitec) regarding drugs incorporated into the SUS (Brazilian Unified Health System) in the period from 2012 to 2024.
Methods: This is an exploratory, descriptive, retrospective study, based on document analysis of Conitec's technical recommendation reports with decisions on the incorporation of drugs published up to 2024. Information from the Budget Impact Analyses (BIA) was extracted and presented in terms of percentage, median and interquartile range.
Nano Lett
September 2025
Pillar of Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, Singapore 487372, Singapore.
Precise delivery of nanoliter-scale reagents is essential for high-throughput biochemical assays, yet existing platforms often lack real-time control and selective content fusion. Conventional methods rely on passive encapsulation or stochastic pairing, limiting both throughput and biochemical specificity. Here, we introduce an on-demand nanoliter delivery platform that seamlessly integrates electrical sensing, triggered droplet merging, and passive sorting in a single continuous flow.
View Article and Find Full Text PDFNanoscale Horiz
September 2025
CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Chinese Academy of Sciences and National Center for Nanoscience and Technology of China, Beijing 100190, China.
Central nervous system (CNS) diseases, including neurodegenerative diseases, stroke, brain tumors, and others, result in poor quality of life and can cause substantial disability. Not all CNS diseases are amenable to surgical approaches, so drug development is important for disease treatment. Unfortunately, there are few drugs currently available for CNS diseases.
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