Alcalá-Alcalá Sergio, Casarrubias-Anacleto José Eduardo, Mondragón-Guillén Maximiliano, Tavira-Montalvan Carlos Alberto, Bonilla-Hernández Marcos, Gómez-Galicia Diana Lizbeth, Gosset Guillermo, Meneses-Acosta Angélica
Laboratorio de Investigación en Tecnología Farmacéutica, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos, Cuernavaca 62209, Morelos, Mexico.
Laboratorio de Biotecnología Farmacéutica, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos, Cuernavaca 62209, Morelos, Mexico.
Polymers (Basel). 2023 May 19;15(10):2381. doi: 10.3390/polym15102381.
Melanin is an insoluble, amorphous polymer that forms planar sheets that aggregate naturally to create colloidal particles with several biological functions. Based on this, here, a preformed recombinant melanin (PRM) was utilized as the polymeric raw material to generate recombinant melanin nanoparticles (RMNPs). These nanoparticles were prepared using (nanocrystallization-NC, and double emulsion-solvent evaporation-DE) and (high-pressure homogenization-HP) manufacturing approaches. The particle size, Z-potential, identity, stability, morphology, and solid-state properties were evaluated. RMNP biocompatibility was determined in human embryogenic kidney (HEK293) and human epidermal keratinocyte (HEKn) cell lines. RMNPs prepared by NC reached a particle size of 245.9 ± 31.5 nm and a Z-potential of -20.2 ± 1.56 mV; 253.1 ± 30.6 nm and -39.2 ± 0.56 mV compared to that obtained by DE, as well as RMNPs of 302.2 ± 69.9 nm and -38.6 ± 2.25 mV using HP. Spherical and solid nanostructures in the approaches were observed; however, they were an irregular shape with a wide size distribution when the HP method was applied. Infrared (IR) spectra showed no changes in the chemical structure of the melanin after the manufacturing process but did exhibit an amorphous crystal rearrangement according to calorimetric and PXRD analysis. All RMNPs presented long stability in an aqueous suspension and resistance to being sterilized by wet steam and ultraviolet (UV) radiation. Finally, cytotoxicity assays showed that RMNPs are safe up to 100 μg/mL. These findings open new possibilities for obtaining melanin nanoparticles with potential applications in drug delivery, tissue engineering, diagnosis, and sun protection, among others.
黑色素是一种不溶性的无定形聚合物,它形成平面片层,这些片层自然聚集形成具有多种生物学功能的胶体颗粒。基于此,本文利用预制重组黑色素(PRM)作为聚合物原料来制备重组黑色素纳米颗粒(RMNP)。这些纳米颗粒采用(纳米结晶法-NC和双乳液-溶剂蒸发法-DE)以及(高压均质法-HP)制造工艺制备。对颗粒大小、Zeta电位、特性、稳定性、形态和固态性质进行了评估。在人胚胎肾(HEK293)和人表皮角质形成细胞(HEKn)细胞系中测定了RMNP的生物相容性。通过NC制备的RMNP粒径为245.9±31.5nm,Zeta电位为-20.2±1.56mV;与通过DE制备的相比,分别为253.1±30.6nm和-39.2±0.56mV,而采用HP制备的RMNP粒径为302.2±69.9nm,Zeta电位为-38.6±2.25mV。在上述方法中观察到球形和固态纳米结构;然而,采用HP方法时,它们形状不规则,粒径分布较宽。红外(IR)光谱显示,制造过程后黑色素的化学结构没有变化,但根据量热法和粉末X射线衍射(PXRD)分析,确实表现出无定形晶体重排。所有RMNP在水悬浮液中都具有长期稳定性,并且耐湿蒸汽和紫外线(UV)辐射灭菌。最后,细胞毒性试验表明,RMNP在浓度高达100μg/mL时是安全的。这些发现为获得在药物递送、组织工程、诊断和防晒等方面具有潜在应用的黑色素纳米颗粒开辟了新的可能性。