Rosa Elisabetta, Carniato Fabio, Tei Lorenzo, Diaferia Carlo, Morelli Giancarlo, Botta Mauro, Accardo Antonella
Department of Pharmacy, Research Centre on Bioactive Peptides (CIRPeB), University of Naples "Federico II", Via Montesano 49, 80131 Naples, Italy.
Department of Science and Technological Innovation, University of Piemonte Orientale "A. Avogadro", Viale T. Michel 11, 15121 Alessandria, Italy.
Pharmaceuticals (Basel). 2022 Dec 16;15(12):1572. doi: 10.3390/ph15121572.
New peptide-based hydrogels incorporating Gd(III) chelates with different hydration states, molecular structures and overall negative charges ([Gd(BOPTA)]2−), [Gd(DTPA)]2−, and ([Gd(AAZTA)]−) were prepared and characterized. N-terminal Fmoc- or acetyl-derivatized hexapeptides (K1, K2 and K3) containing five aliphatic amino acids (differently ordered Gly, Ala, Val, Leu and Ile) and a charged lysine at the amidated C-terminal were used for the formation of the hydrogels. Particular attention was paid to the investigation of the morphological and rheological properties of the nanoparticles, in addition to the assessment of the ability (relaxivity) of the confined complexes to accelerate the longitudinal relaxation rate of the water protons localized in the polymeric network. The relaxivity values at high magnetic fields (>0.5 T) of the paramagnetic hydrogels appear to be more than five times higher than those of isolated chelates in an aqueous solution, reaching a value of 25 mmol−1 s−1 for Fmoc-K2+[Gd(BOPTA)]2− at 0.5 T and 310 K. Furthermore, an interesting trend of decrease of relaxivity with increasing the degree of rigidity of the hydrogel was observed. The type of interactions between the various complexes and the polymeric network also plays a key role in influencing the relaxivity values of the final materials. Nanogels were also obtained from the submicronization of the hydrogel containing [Gd(BOPTA)]2− chelate. Circular dichroism, dynamic light scattering and relaxometric investigations on these nanoparticles revealed the formation of nanogels endowed with higher relaxivities (r1 = 41 mM−1 s−1 at 0.5 T MHz and 310 K) than the corresponding hydrogels.
制备并表征了新型肽基水凝胶,其包含具有不同水合状态、分子结构和整体负电荷的钆(III)螯合物([Gd(BOPTA)]2−、[Gd(DTPA)]2−和([Gd(AAZTA)]−)。N端经芴甲氧羰基(Fmoc)或乙酰基衍生化的六肽(K1、K2和K3),含有五个脂肪族氨基酸(甘氨酸、丙氨酸、缬氨酸、亮氨酸和异亮氨酸排列不同)以及在酰胺化C端的一个带电荷赖氨酸,用于形成水凝胶。除了评估受限配合物加速聚合物网络中水质子纵向弛豫速率的能力(弛豫率)外,还特别关注了纳米颗粒的形态学和流变学性质研究。顺磁性水凝胶在高磁场(>0.5 T)下的弛豫率值似乎比水溶液中分离的螯合物高五倍以上,在0.5 T和310 K时,Fmoc-K2+[Gd(BOPTA)]2−的弛豫率值达到25 mmol−1 s−1。此外,观察到弛豫率随水凝胶刚性程度增加而降低的有趣趋势。各种配合物与聚合物网络之间的相互作用类型在影响最终材料的弛豫率值方面也起着关键作用。还通过含[Gd(BOPTA)]2−螯合物的水凝胶亚微粉化得到了纳米凝胶。对这些纳米颗粒的圆二色性、动态光散射和弛豫测量研究表明,所形成的纳米凝胶具有比相应水凝胶更高的弛豫率(在0.5 T MHz和310 K时r1 = 41 mM−1 s−1)。