AI Article Synopsis

  • HIV-1 infections lead to serious health issues globally, highlighting the need for innovative drug delivery systems using nanotechnology.
  • Researchers developed a new negatively charged G2 dendrimer nano-biopolymer that was conjugated with anti-HIV drugs lamivudine and efavirenz, utilizing various analytical methods for characterization.
  • In tests on HIV-infected cells, lamivudine showed a significant reduction in viral activity without harming cells, while efavirenz also demonstrated effectiveness, suggesting these nano-constructs are promising for future anti-HIV research.

Article Abstract

Infection with human immunodeficiency virus (HIV)-1 causes immunological disorders and death worldwide which needs to be further assisted by novel anti-retroviral drug delivery systems. Consequently, finding newer anti-retroviral pharmaceuticals by using biocompatible, biodegradable nanomaterials comprising a nanoparticle as core and a therapeutic agent is of high global interest. In this experiment, a second generation of a negatively charged nano-biopolymer linear globular G2 dendrimer was carefully conjugated and loaded with well-known anti-HIV drugs lamivudine and efavirenz, respectively. They were characterised by a variety of analytical methods such as Zetasizer, Fourier-transform infrared spectroscopy, elemental analysis and liquid chromatography-mass spectroscopy. Additionally, conjugated lamivudine and loaded efazirenz with globular PEGylated G2 dendrimer were tested on an HEK293 T cell infected by single-cycle replicable HIV-1 virion and evaluated using XTT test and HIV-1 P24 protein load. The results showed that lamivudine-conjugated G2 significantly decreased retroviral activity without any cell toxicity. This effect was more or less observed by efavirenz-loaded G2. These nano-constructs are strongly suggested for further in vivo anti-HIV assays.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675833PMC
http://dx.doi.org/10.1049/nbt2.12060DOI Listing

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