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Lactoferrin bioconjugated solid lipid nanoparticles: a new drug delivery system for potential brain targeting

机译:Lactoferrin Bioconjugated固体脂质纳米颗粒:一种用于潜在脑靶向的新药递送系统

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Background: Delivery of drugs to brain is a subtle task in the therapy of many severe neurological disorders. Solid lipid nanoparticles (SLN) easily diffuse the blood-brain barrier (BBB) due to their lipophilic nature. Furthermore, ligand conjugation on SLN surface enhances the targeting efficiency. Lactoferin (Lf) conjugated SLN system is first time attempted for effective brain targeting in this study.Purpose: Preparation of Lf-modified docetaxel (DTX)-loaded SLN for proficient delivery of DTX to brain.Methods: DTX-loaded SLN were prepared using emulsification and solvent evaporation method and conjugation of Lf on SLN surface (C-SLN) was attained through carbodiimide chemistry. These lipidic nanoparticles were evaluated by DLS, AFM, FTIR, XRD techniques and in vitro release studies. Colloidal stability study was performed in biologically simulated environment (normal saline and serum). These lipidic nanoparticles were further evaluated for its targeting mechanism for uptake in brain tumour cells and brain via receptor saturation studies and distribution studies in brain, respectively.Results: Particle size of lipidic nanoparticles was found to be optimum. Surface morphology (zeta potential, AFM) and surface chemistry (FTIR) confirmed conjugation of Lf on SLN surface. Cytotoxicity studies revealed augmented apoptotic activity of C-SLN than SLN and DTX. Enhanced cytotoxicity was demonstrated by receptor saturation and uptake studies. Brain concentration of DTX was elevated significantly with C-SLN than marketed formulation.Conclusions: It is evident from the cytotoxicity, uptake that SLN has potential to deliver drug to brain than marketed formulation but conjugating Lf on SLN surface (C-SLN) further increased the targeting potential for brain tumour. Moreover, brain distribution studies corroborated the use of C-SLN as a viable vehicle to target drug to brain. Hence, C-SLN was demonstrated to be a promising DTX delivery system to brain as it possessed remarkable biocompatibility, stability and efficacy than other reported delivery systems.
机译:背景:将药物交付给脑中是许多严重神经系统疾病治疗的微妙任务。固体脂质纳米颗粒(SLN)由于其亲脂性本质而容易地扩散血脑屏障(BBB)。此外,SLN表面上的配体缀合增强了靶向效率。乳蛋白酶(LF)共轭SLN系统首次尝试在本研究中试图有效脑靶向。用于制备LF改性的多西紫杉醇(DTX) - 载荷的SLN,用于易于递送DTX至脑。方法:使用DTX加载的SLN通过碳二亚胺化学获得乳化和溶剂蒸发方法和LF上的LF缀合物。通过DLS,AFM,FTIR,XRD技术和体外释放研究评估这些脂质纳米颗粒。在生物模拟环境(正常盐水和血清)中进行胶体稳定性研究。进一步评估这些脂质纳米颗粒,用于通过脑中受体饱和研究和脑的脑肿瘤细胞和脑吸收的靶向机制。结果:发现脂质纳米颗粒的粒度是最佳的。表面形态(Zeta电位,AFM)和表面化学(FTIR)证实了LF在SLN表面上的缀合。细胞毒性研究显示C-SLN的增强凋亡活性而不是SLN和DTX。受体饱和度和摄取研究证明了增强的细胞毒性。 DTX的脑浓度明显高于销售制剂的C-SLN。结论:从细胞毒性明显看出,SLN具有将药物递送到脑中的潜力而不是销售制剂,但在SLN表面(C-SLN)上缀合LF进一步增加脑肿瘤的靶向潜力。此外,脑分布研究证实了C-SLN作为可行载体的使用以将药物靶向脑。因此,C-SLN被证明是对大脑的有前途的DTX递送系统,因为它具有显着的生物相容性,稳定性和功效而不是其他报告的递送系统。

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