Application of Strontium Chloride Hexahydrate to Synthesize Strontium-Substituted Carbonate Apatite as a pH-Sensitive, Biologically Safe, and Highly Efficient siRNA Nanocarrier.

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2025-01-20 Epub Date: 2024-12-26 DOI:10.1021/acsabm.4c01319
Fatema Tuz Zohora, Rajadurai Pathmanathan, Ezharul Hoque Chowdhury
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引用次数: 0

Abstract

Naked siRNAs are sensitive to enzymatic degradation, phagocytic entrapment, quick renal excretion, membrane impermeability, endosomal escape, and off-target effects. Designing a safe and efficient nanocarrier for siRNA delivery to the target site without toxicity remains a significant hurdle in gene therapy. CA is a unique derivative of hydroxyapatite and a highly pH-sensitive nanocarrier with strong particle aggregation and a high polydispersity index. Strontium (Sr2+), a group two divalent metal in the periodic table, has been reported for substituting calcium (Ca2+) ions from the apatite lattice and limiting particle growth/aggregation. This study used strontium chloride hexahydrate (SrCl2·6H2O) salt to develop a Sr-substituted CA (Sr-CA) nanocarrier with ∼30 nm size, spherical shape, less aggregation, homodispersity, and a fair anionic charge. Sr-CA demonstrated a large surface area-to-volume ratio, an improved cargo loading efficiency, and enhanced cellular uptake in HEK-293 cells. Moreover, Sr-CA is a pH-responsive nanocarrier responsible for its long physiological stability, efficient endosomal escape, and optimal cargo delivery within cells. These NPs have differential effects on MAPK1, MAP2K4, PIK3Ca, CAMK4, and p53 gene expression in HEK-293 cells without showing any significant cytotoxicity in cell growth properties. Gene silencing by Sr-CA-mediated siRNA delivery against MAPK1, MAP2K4, PIK3Ca, and CAMK4 genes significantly decreased the level of target gene expression and cell survival, demonstrating successful intracellular siRNA delivery in HEK-293 cells. Additionally, biocompatibility testing confirmed the biological safety of the Sr-CA nanocarrier in mice. These findings suggest that Sr-CA nanocarriers are a promising siRNA delivery system, combining high efficiency with pH-sensitive release and excellent biocompatibility, making them a viable option for future therapeutic applications.

应用六水氯化锶合成锶取代碳酸盐磷灰石作为ph敏感、生物安全、高效的siRNA纳米载体。
裸sirna对酶降解、吞噬包裹、肾脏快速排泄、膜不透性、内体逃逸和脱靶效应敏感。设计一种安全有效的纳米载体将siRNA无毒性地递送到靶点仍然是基因治疗的一个重大障碍。CA是一种独特的羟基磷灰石衍生物,是一种对ph值高度敏感的纳米载体,具有很强的颗粒聚集性和高多分散指数。锶(Sr2+)是元素周期表中的一种二价金属,据报道可以取代磷灰石晶格中的钙(Ca2+)离子,并限制颗粒的生长/聚集。本研究使用六水氯化锶(SrCl2·6H2O)盐制备了一种尺寸为~ 30 nm的sr -取代CA (Sr-CA)纳米载体,该载体具有球形、聚集性低、均匀分散性好、阴离子电荷均匀等特点。Sr-CA在HEK-293细胞中表现出较大的表面积体积比,提高了货物装载效率,并增强了细胞摄取。此外,Sr-CA是一种ph响应型纳米载体,具有长期的生理稳定性、高效的内体逃逸和最佳的细胞内货物递送。这些NPs对HEK-293细胞中的MAPK1、MAP2K4、PIK3Ca、CAMK4和p53基因表达有不同的影响,但对细胞生长特性没有明显的细胞毒性。通过sr - ca介导的靶向MAPK1、MAP2K4、PIK3Ca和CAMK4基因的siRNA传递沉默基因,可显著降低靶基因的表达水平和细胞存活率,证明siRNA在HEK-293细胞内传递成功。此外,生物相容性试验证实了Sr-CA纳米载体在小鼠体内的生物安全性。这些发现表明,Sr-CA纳米载体是一种很有前途的siRNA递送系统,结合了高效率、ph敏感释放和良好的生物相容性,使其成为未来治疗应用的可行选择。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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