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The Most Cited Literature on Block Copolymer Micelles
Block copolymer micelles are generally formed by the self-assembly of either amphiphilic or oppositely charged copolymers in aqueous medium. In this article, the editor summarizes the most cited research results that scientists have made on block copolymer micelles, and hope you can find what you need. What are Block Copolymer Micelles? Block copolymer micelles are generally formed by the self-assembly of either amphiphilic or oppositely charged copolymers in aqueous medium. The hydrophilic and hydrophobic blocks form the corona and the core of the micelles, respectively. The presence of a nonionic water-soluble shell as well as the scale (10-100 nm) of polymeric micelles are expected to restrict their uptake by the mononuclear phagocyte system and…
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Want a Quick Q&A for Exosomes? Read This!
In recent years, biomimetic nanomedicine combined with the unique functions of natural biomaterials and the versatility of artificial nanomaterials has attracted widespread attention for drug delivery. In 2019, the study Tumor exosome-based nanoparticles are efficient drug carriers for chemotherapy published in Nature Communications have showed that exosomes-biomimetic nanoparticles have the potential to improve anti-cancer efficacy as drug carriers. Moreover, because such nanoparticles can effectively kill tumor stem cells, it is expected to solve major problems such as tumor recurrence, metastasis and drug resistance. Exosomes are cell vesicles that contain complex RNA and proteins. Their size is in the nanometer range (30-150 nanometers in diameter), and they can be secreted by a variety of cells under…
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In Vivo Characteristics of Antitumor Drug Liposomes
Anti-tumor drug liposomes need to be studied in vivo during the development process, which includes examination of liposome pharmacokinetics, clinical efficacy and in vivo safety. Pharmacokinetics Liposomes have a greater influence on the pharmacokinetic parameters of drug-loaded drugs, which are characterized by increased AUC(area under the curve, it shows drug’s bioavailabilit), extended half-life period, decreased clearance, decreased volume of distribution, and changes in tissue distribution. The pharmacological changes can be explained and proven from the anatomical characteristics of tumor sites, structural characteristics of liposomes, non-clinical studies and clinical studies. The targeting of liposomes is divided into passive targeting, physicochemical targeting and active targeting. These targeting effects make the pharmacokinetic behavior of liposome…
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Application Prospects of Targeted Nano Drug Delivery System
Targeted drugs were proposed by German scientist and Nobel Prize winner Ehrlich in 1906 and have a history of more than 100 years. Until the late 1970s, with the advancement of molecular biology, cell biology, and materials science, targeted formulations developed rapidly, and products began to be marketed. The nano drug delivery system is distributed in specific organs, tissues, cells, and even intracellular structures in the body through passive targeting, active targeting, physical and chemical targeting, etc., and changes the distribution of prototype drugs in vivo. With the leapfrog development of life sciences, human understanding of disease pathogenesis and drug action mechanisms has transitioned from a macroscopic overall level to…
