4.7 Article

Biocompatible Assessment of Erythrocyte Membrane-Camouflaged Polymeric PLGA Nanoparticles in Pregnant Mice: Both on Maternal and Fetal/Juvenile Mice

期刊

INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 17, 期 -, 页码 5899-5913

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S384906

关键词

erythrocyte membrane; pregnancy; fetus; biocompatibility; RNA sequencing

资金

  1. Outstanding Youth Fund Project of Zhejiang Natural Science Foundation [LR22H150001]
  2. Key Projects Jointly Constructed by Zhejiang Province and the Ministry [WKJ-ZJ-2339]
  3. Major Innovation Project of Wenzhou Science and Technology Bureau [2021ZY0002]
  4. Natural Science Foundation of China [81701828, 82071626]
  5. WenZhou DaTong Biotech Co., Ltd (Wenzhou, China)

向作者/读者索取更多资源

This study evaluated the biocompatibility and safety of red blood cell-membrane coated nanoparticles in pregnant mice and their offspring. The results showed that these nanoparticles were generally safe and biocompatible for both maternal mice during pregnancy and subsequent juvenile mice post-birth, although further studies are needed to examine higher dosage or longer-term measurements.
Purpose: Poly(lactic-co-glycolic) acid (PLGA) nanoparticles coated with the membrane of red blood cells (RBC-NP) have been applied in various biomedical fields. Despite the well-documented great biocompatibility, the potential toxicity of RBC-NP on maternal mice or their developing fetuses during pregnancy, or juvenile mice post-birth, remains unclear, which warrants a systematic evaluation. Methods: We fabricate an RBC-NP with approximately 50 nm in diameter (RBC-NP-50). Upon RBC-NP-50, pregnant mice are intravenously injected with this nanoparticle either at a single high dose of 400 mg/kg (1HD) or a low dose of 200 mg/kg for 3 times (3LD). Afterwards, the biocompatible assessments are performed at 48 h after the final injection or 21 d post-birth/partum both on maternal and fetal/juvenile mice. Results: RBC-NP-50 is capable of accumulating in the placenta and then passing through the blood-fetal barrier (BFB) into the fetus. On 48 h after RBC-NP-50 exposure, no significant dose-dependent toxicity is observed in maternal mice including blood biochemistry, inflammatory factors, progesterone level, histological analysis, etc, whereas fetal brains reveal remarkable differentially expressed genes analyzed by transcriptome sequencing. On 21 d post-birth, those genes' expression in juvenile mice is alleviated, along with negligible differences in behavioral evaluations including surface righting test, negative geotaxis test, cliff avoidance test, and olfactory orientation test. Conclusion: These results indicate that RBC-NP is considered to be generally safe and biocompatible both for maternal mice and fetus during pregnancy, and for the subsequent juvenile mice post-birth, although future studies will need to examine higher dosage or longer-term measurements.

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