Lazar Geza, Nekvapil Fran, Hirian Razvan, Glamuzina Branko, Tamas Tudor, Barbu-Tudoran Lucian, Pinzaru Simona Cinta
Biomolecular Physics Department, Babes Bolyai University, Kogalniceanu 1, RO-400084 Cluj-Napoca, Romania.
Institute for Research, Development and Innovation in Applied Natural Science, Fântânele 30, 400327 Cluj-Napoca, Romania.
ACS Omega. 2021 Oct 11;6(42):27781-27790. doi: 10.1021/acsomega.1c03285. eCollection 2021 Oct 26.
The ever-growing demand for novel, cheaper, and more effective drugs has put nanomedicine and targeted drug delivery to the forefront of scientific innovation. Owing to its porous three-dimensional (3D)-nanostructure and properties, the biogenic calcite from wasted blue crab shells is employed in the present work as a new drug carrier for 5-fluorouracil (5-FU), a drug widely used in cancer therapy. The drug solution has been loaded in the porous nanoarchitecture of the powdered biogenic material and further pelleted in tablets with a 5-FU concentration of 1.748 mg/g. Their structural and morphological properties were characterized using Raman, X-ray diffraction, and scanning electron microscopy. Confocal micro-Raman spectra of tablet surface showed a typical signal of biogenic carbonate with preserved carotenoids and carotenoproteins found in the native waste shell, while the drug Raman signal was absent, indicating its adsorption in the intricate nanoporous biogenic carrier. The slow release of the drug from the newly formulated tablet was investigated by tracking the surface-enhanced Raman scattering (SERS) signal of the tablet solution in a series of time-dependent experiments. The SERS signal quantification is achieved using the well-known SERS spectral fingerprint of 5-fluorouracil aqueous solution adsorbed on Ag nanoparticles. The proof of concept is demonstrated by quantifying the slow release of the drug through the characteristic SERS band intensity of 5-FU in a time course of 26 h. This proof of concept boosted further investigations concerning the released drug identity in simulated solutions that mimic the pH of the upper- and lower gastrointestinal tract, as well as the multiple possibilities to control porosity and composition during powdering and treatment of biogenic material, to achieve the most convenient formulation for relevant biomedical drug delivery. Nonetheless, the present results showed great promise for innovative reusing waste biogenic 3D-nanomaterials of aquatic origin as advantageous drug carriers for slow release purposes, in line with the concept of blue bioeconomy.
对新型、更廉价且更有效的药物的需求不断增长,使得纳米医学和靶向药物递送成为科学创新的前沿领域。由于其多孔三维(3D)纳米结构和特性,本研究采用废弃蓝蟹壳中的生物成因方解石作为5-氟尿嘧啶(5-FU)的新型药物载体,5-FU是一种广泛用于癌症治疗的药物。药物溶液被载入粉末状生物材料的多孔纳米结构中,并进一步制成片剂,其中5-FU浓度为1.748 mg/g。使用拉曼光谱、X射线衍射和扫描电子显微镜对其结构和形态特性进行了表征。片剂表面的共聚焦显微拉曼光谱显示出生物成因碳酸盐的典型信号,同时保留了天然废壳中发现的类胡萝卜素和类胡萝卜素蛋白,而药物拉曼信号缺失,表明其吸附在复杂的纳米多孔生物载体中。通过在一系列时间依赖性实验中跟踪片剂溶液的表面增强拉曼散射(SERS)信号,研究了新制备片剂中药物的缓释情况。使用吸附在银纳米颗粒上的5-氟尿嘧啶水溶液的著名SERS光谱指纹实现SERS信号定量。通过在26小时的时间过程中通过5-FU的特征SERS带强度定量药物的缓慢释放,证明了概念验证。这一概念验证推动了进一步的研究,涉及模拟上消化道和下消化道pH值的模拟溶液中释放药物的身份,以及在生物材料的粉末化和处理过程中控制孔隙率和组成的多种可能性,以实现相关生物医学药物递送的最便捷配方。尽管如此,目前的结果显示出将水生来源的废弃生物成因3D纳米材料创新地重新用作缓释目的的有利药物载体的巨大潜力,这与蓝色生物经济的概念一致。