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

被引:4
|
作者
Chen, Sailing [1 ]
Tian, Dongyan [1 ]
Yang, Xuewei [1 ]
Yin, Qingqing [1 ]
Li, Li [1 ]
Lin, Yijing [1 ]
Liu, Shuangshuang [1 ]
Chen, Huiqian [1 ]
Zhang, Mingyao [1 ]
Lin, Jiajin [2 ]
Lu, Xiaosheng [1 ]
Duan, Ping [1 ]
Chen, Yijie [1 ,3 ,4 ]
机构
[1] Wenzhou Med Univ, Dept Obstet & Gynecol, Affiliated Hosp 2, 109 West Xueyuan Rd, Wenzhou 325027, Peoples R China
[2] Wenzhou Med Univ, Dept Blood Transfus, Affiliated Hosp 2, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, Cixi Biomed Res Inst, Wenzhou, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 2, Zhejiang Engn Res Ctr Innovat & Applicat Intellig, 109 West Xueyuan Rd, Wenzhou 325027, Zhejiang, Peoples R China
来源
基金
浙江省自然科学基金;
关键词
erythrocyte membrane; pregnancy; fetus; biocompatibility; RNA sequencing; DRUG-DELIVERY; RBC MEMBRANES; SAFE;
D O I
10.2147/IJN.S384906
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:5899 / 5913
页数:15
相关论文
共 8 条
  • [1] Erythrocyte membrane-camouflaged polymeric nanoparticles as a biomimetic delivery platform
    Hu, Che-Ming J.
    Zhang, Li
    Aryal, Santosh
    Cheung, Connie
    Fang, Ronnie H.
    Zhang, Liangfang
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (27) : 10980 - 10985
  • [2] Erythrocyte Membrane-Camouflaged Aggregation-Induced Emission Nanoparticles for Fetal Intestinal Maturation Assessment
    Dai, Jun
    Chen, Zhaojun
    Chen, Biao
    Dong, Xiyuan
    Wu, Meng
    Lou, Xiaoding
    Xia, Fan
    Wang, Shixuan
    ANALYTICAL CHEMISTRY, 2022, 94 (50) : 17504 - 17513
  • [3] Erythrocyte membrane-camouflaged nanoparticles as effective and biocompatible platform: Either autologous or allogeneic erythrocyte-derived
    Dai, Jun
    Chen, Zhaojun
    Wang, Shixuan
    Xia, Fan
    Lou, Xiaoding
    MATERIALS TODAY BIO, 2022, 15
  • [4] Erythrocyte Membrane-Camouflaged IR780 and DTX Coloading Polymeric Nanoparticles for Imaging-Guided Cancer Photo-Chemo Combination Therapy
    Yang, Qian
    Xiao, Yao
    Yin, Yanlong
    Li, Gaoyin
    Peng, Jinrong
    MOLECULAR PHARMACEUTICS, 2019, 16 (07) : 3208 - 3220
  • [5] Red blood cell membrane-camouflaged vancomycin and chlorogenic acid-loaded gelatin nanoparticles against multi-drug resistance infection mice model
    Kamal, Zul
    Su, Jing
    Yuan, Weien
    Raza, Faisal
    Jiang, Liangdi
    Li, Yichen
    Qiu, Mingfeng
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2022, 76
  • [6] Mannose-modified erythrocyte membrane-coated Chuanmingshen violaceum polysaccharide PLGA nanoparticles to improve immune responses in mice
    Yang, Shuyao
    Zhang, Xinnan
    Wang, Yao
    Liu, Jie
    Wang, Lu
    Liao, Yi
    Yang, Yanwen
    Dai, Tao
    Yin, Xuemei
    Li, Shanshan
    Han, Lu
    Zhu, Jiangjiang
    Feng, Haibo
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2025, 152
  • [7] Erythrocyte Membrane-Camouflaged IR780 and DTX Coloading Polymeric Nanoparticles for Imaging-Guided Cancer Photo-Chemo Combination Therapy (vol 16, pg 3208, 2019)
    Yang, Qian
    Xiao, Yao
    Yin, Yanlong
    Li, Gaoyin
    Peng, Jinrong
    MOLECULAR PHARMACEUTICS, 2019, 16 (09) : 4086 - 4086
  • [8] Size-dependent maternal-fetal transfer and fetal developmental toxicity of ZnO nanoparticles after oral exposures in pregnant mice
    Teng, Chuanfeng
    Jia, Jianbo
    Wang, Zhiping
    Sharma, Virender K.
    Yan, Bing
    ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2019, 182