4.6 Article

Multi-Dose Intravenous Administration of Neutral and Cationic Liposomes in Mice: An Extensive Toxicity Study

期刊

PHARMACEUTICALS
卷 15, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/ph15060761

关键词

lipid-based nanoparticles; nanocarrier; surface charge; delivery systems; chronic treatment; mice

资金

  1. FCT/MCTES (PIDDAC) [LA/P/0045/2020, UIDP/00511/2020]
  2. Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement [NORTE-01-0145FEDER-000054]
  3. European Regional Development Fund (ERDF)
  4. FCT-Fundacao para a Ciencia e a Tecnologia [EXPL/NAN-MAT/0209/2021]
  5. FCT [SFRH/BD/129312/2017, COVID/BD/151869/2021]
  6. Scientific Employment Stimulus-Institutional Call [CEECINST/00049/2018]
  7. NIH [1RF1AG059321-01A1]
  8. Fundação para a Ciência e a Tecnologia [EXPL/NAN-MAT/0209/2021, COVID/BD/151869/2021] Funding Source: FCT

向作者/读者索取更多资源

This study evaluated the toxicity of prolonged administration of liposomes composed of neutral or cationic phospholipids. The results showed that cationic liposomes were toxic, leading to higher mortality and negative effects on motor function and inflammation, whereas neutral liposomes did not exhibit toxicity.
Liposomes are widely used as delivery systems for therapeutic purposes. However, the toxicity associated with the multi-dose administration of these nanoparticles is not fully elucidated. Here, we evaluated the toxicity of the prolonged administration of liposomes composed of neutral or cationic phospholipids often used in drug and gene delivery. For that purpose, adult wild-type mice (C57Bl6) were randomly distributed into three groups receiving either vehicle (PBS), neutral, or cationic liposomes and subjected to repeated intravenous injections for a total of 10 doses administered over 3 weeks. Several parameters, including mortality, body weight, and glucose levels, were monitored throughout the trial. While these variables did not change in the group treated with neutral liposomes, the group treated with the positively charged liposomes displayed a mortality rate of 45% after 10 doses of administration. Additional urinalysis, blood tests, and behavioral assays to evaluate impairments of motor functions or lesions in major organs were also performed. The cationic group showed less forelimb peak force than the control group, alterations at the hematological level, and inflammatory components, unlike the neutral group. Overall, the results demonstrate that cationic liposomes are toxic for multi-dose administration, while the neutral liposomes did not induce changes associated with toxicity. Therefore, our results support the use of the well-known neutral liposomes as safe drug shuttles, even when repetitive administrations are needed.

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