Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 96, P. 105709 - 105709
Published: April 25, 2024
Language: Английский
Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 96, P. 105709 - 105709
Published: April 25, 2024
Language: Английский
Molecules, Journal Year: 2024, Volume and Issue: 29(6), P. 1199 - 1199
Published: March 7, 2024
Cardiovascular disease (CVD) stands as the foremost cause of patient mortality, and lack early diagnosis defined treatment targets significantly contributes to suboptimal prevention management CVD. Myocardial fibrosis (MF) is not only a complex pathogenic process with no effective currently available but also exerts detrimental effects on progression various cardiovascular diseases, thereby escalating their mortality rates. Exosomes are nanoscale biocommunication vehicles that facilitate intercellular communication by transporting bioactive substances, such nucleic acids proteins, from specific cell types. Numerous studies have firmly established microRNAs (miRNAs), non-coding RNAs, wield post-transcriptional regulatory mechanisms exhibit close associations CVDs, including coronary heart (CHD), atrial fibrillation (AF), failure (HF). MiRNAs hold significant promise in diseases. In this review, we provide concise introduction biological attributes exosomes exosomal miRNAs. We explore roles distinct cell-derived miRNAs context myocardial fibrosis. These findings underscore pivotal role cardiac emphasize potential biotherapies drug delivery vectors for treatment.
Language: Английский
Citations
7Biomaterials, Journal Year: 2024, Volume and Issue: 308, P. 122544 - 122544
Published: March 31, 2024
Language: Английский
Citations
7International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 663, P. 124547 - 124547
Published: Aug. 2, 2024
Language: Английский
Citations
7Colloids and Interface Science Communications, Journal Year: 2024, Volume and Issue: 59, P. 100775 - 100775
Published: Feb. 23, 2024
Myocardial infarction (MI) is a typical cardiovascular disease, causing disability and death worldwide. Exosomes secreted by mesenchymal stem cells (MSCs) showed remarkable therapeutic effects in MI restoring cardiac function. However, the application of exosomes remains challenge because their low residence rate infarcted myocardium. Herein, fibrin-based patch was prepared to deliver MSCs-derived heart using an mouse model, aiming at improvement functions. The fibrin optimized for size minimize mortality rate. composite sustained release vitro could improve retention heart, inhibiting fibrosis improving functions vivo. Therefore, this combination natural biomaterial-based may have promising clinical translational potential treatment.
Language: Английский
Citations
6Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 96, P. 105709 - 105709
Published: April 25, 2024
Language: Английский
Citations
6