Biomimetic camouflaged nanoparticles with selective cellular internalization and migration competences

被引:6
作者
Jimenez-Jimenez, Carla [1 ,2 ]
Moreno-Borrallo, Almudena [1 ]
Dumontel, Bianca [1 ]
Manzano, Miguel [1 ,2 ]
Vallet-Regi, Maria [1 ,2 ]
机构
[1] Univ Complutense Madrid, Inst Hosp 12 Octubre Imas12, Sch Pharm, Dept Chem Pharmaceut Sci, Madrid 28040, Spain
[2] Networking Res Ctr Bioengn Biomat & Nanomed CIBER, Madrid 28029, Spain
基金
欧洲研究理事会;
关键词
Nanomedicine; Coating technology; Cell membranes; Nanocarriers for drug delivery; MESOPOROUS SILICA; DRUG-DELIVERY; ERYTHROCYTE-MEMBRANE; MCM-41; CELLS; NANOSYSTEM; THERAPY;
D O I
10.1016/j.actbio.2022.11.059
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In the last few years, nanotechnology has revolutionized the potential treatment of different diseases. However, the use of nanoparticles for drug delivery might be limited by their immune clearance, poor biocompatibility and systemic immunotoxicity. Hypotheses for overcoming rejection from the body and increasing their biocompatibility include coating nanoparticles with cell membranes. Additionally, source cell-specific targeting has been reported when coating nanoparticles with tumor cells membranes. Here we show that coating mesoporous silica nanoparticles with membranes derived from preosteoblastic cells could be employed to develop potential treatments of certain bone diseases. These nanoparticles were se-lected because of their well-established drug delivery features. On the other hand MC3T3-E1 cells were selected because of their systemic migration capabilities towards bone defects. The coating process was here optimized ensuring their drug loading and delivery features. More importantly, our results demon-strated how camouflaged nanocarriers presented cellular selectivity and migration capability towards the preosteoblastic source cells, which might constitute the inspiration for future bone disease treatments.
引用
收藏
页码:395 / 407
页数:13
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