Castro-Balado Ana, Cuartero-Martínez Andrea, Pena-Verdeal Hugo, Hermelo-Vidal Gonzalo, Schmidt Anja, Montero Belén, Hernández-Blanco Manuela, Zarra-Ferro Irene, González-Barcia Miguel, Mondelo-García Cristina, Giráldez María Jesús, Yebra-Pimentel Eva, Otero-Espinar Francisco J, Fernández-Ferreiro Anxo
Pharmacy Department, University Clinical Hospital of Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Clinical Pharmacology Group, Health Research Institute of Santiago de Compostela (IDIS), 15706 Santiago de Compostela, Spain.
Pharmaceutics. 2023 Nov 5;15(11):2589. doi: 10.3390/pharmaceutics15112589.
Cystinosis is a rare genetic disorder characterized by the accumulation of cystine crystals in several tissues and organs causing, among others, severe eye symptoms. The high instability of cysteamine eye drops makes it difficult to develop formulations with an acceptable shelf life to be prepared in hospital pharmacy departments. Previously, a new compounded formulation of cysteamine eye drops in hyaluronic acid (HA) packaged in innovative single-dose systems was developed.
Long-term stability at -20 °C of this formulation was studied considering the content of cysteamine, pH, osmolality, viscosity, and microbiological analysis. The oxygen permeability of single-dose containers was also studied and an ocular biopermanence study was conducted in healthy volunteers measuring lacrimal stability and volume parameters.
Data confirm that cysteamine concentration remained above 90% for 120 days, all parameters remaining within the accepted range for ophthalmic formulations. The permeability of the containers was reduced over time, while ocular biopermanence was maintained despite the freezing process and storage time.
0.55% cysteamine hydrochloride formulation in HA and packaged in single-dose containers preserved at -20 °C is stable for 120 days protected from light, presenting high potential for its translation into clinical practice when commercial presentations are not available.
胱氨酸病是一种罕见的遗传性疾病,其特征是胱氨酸晶体在多个组织和器官中积累,尤其会导致严重的眼部症状。半胱胺滴眼液的高不稳定性使得在医院药房配制具有可接受保质期的制剂变得困难。此前,已开发出一种新的复合制剂,即装在创新单剂量系统中的透明质酸(HA)半胱胺滴眼液。
考虑半胱胺含量、pH值、渗透压、粘度和微生物分析,研究了该制剂在-20°C下的长期稳定性。还研究了单剂量容器的氧气渗透性,并在健康志愿者中进行了眼部生物持久性研究,测量泪液稳定性和体积参数。
数据证实,半胱胺浓度在120天内保持在90%以上,所有参数均保持在眼科制剂的可接受范围内。随着时间的推移,容器的渗透性降低,尽管经过冷冻过程和储存时间,眼部生物持久性仍得以维持。
装在HA中并保存在-20°C的单剂量容器中的0.55%盐酸半胱胺制剂在避光条件下可稳定120天,在没有商业产品的情况下,具有很高的转化为临床应用的潜力。