结膜下注射地塞米松微晶原药,用于超声乳化手术后的长效消炎。

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Controlled Release Pub Date : 2024-11-19 DOI:10.1016/j.jconrel.2024.11.046
Xueyan Zhou, Zunkai Xu, Yanliang Dong, Maoyu Cai, Zhixia Chen, Jingqing Mu, Bo Yuan, Xia Hua, Xiaoyong Yuan, Shutao Guo
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引用次数: 0

摘要

地塞米松的长效微创注射制剂非常适合用于治疗慢性眼部炎症。在此,我们应用疏水性丙酮基酮联地塞米松原药(SKD)的微晶(MCs)来治疗术后眼部炎症。我们比较了通过结膜下注射 SKD MCs 与通过结膜下注射和滴眼液的 Maxidex(地塞米松 MCs 局部混悬液)在超声乳化联合眼内人工晶体植入术(Phaco-IOL)兔模型中的疗效和安全性。在Phaco-IOL兔眼中,单次SKD MCs(0.4毫克地塞米松当量)皮下注射的抗炎效果与Maxidex滴眼液相当,并能在28天内完全缓解炎症,而相同剂量的Maxidex皮下注射仅能提供7天的抗炎效果。对 SKD MCs 抗炎作用剂量依赖性的研究表明,高剂量(0.8 毫克地塞米松当量)和低剂量(0.4 毫克地塞米松当量)的抗炎作用在 28 天内没有显著差异。不过,SKD MCs 和 Maxidex 在正常兔子体内经皮下注射后的系统药物分布情况表明,高剂量的药物在结膜中的浓度更高,而高剂量的 SKD MCs 至少在 84 天后仍可在角膜和虹膜睫状体中检测到相当数量的原药和地塞米松。此外,没有观察到持续的眼压升高以及视网膜结构和厚度异常,这证实了长效 SKD MCs 在注射 SC 后具有极佳的安全性。我们的研究结果为利用基于原药的MCs治疗眼部术后炎症提供了有价值的见解,详细的药物分布分析将促进这些MCs在眼科疾病中的临床转化。
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Subconjunctival injection of microcrystalline prodrug of dexamethasone for long-acting anti-inflammation after phacoemulsification surgery.

Long-acting injectable formulations of dexamethasone with minimal invasiveness are highly desired to manage chronic ocular inflammatory conditions. Here, we applied microcrystals (MCs) of a hydrophobic acetone-based ketal-linked prodrug of dexamethasone (SKD) to treat postoperative ocular inflammation. We compared the efficacy and safety of SKD MCs through subconjunctival (SC) injection with that of Maxidex (a topical suspension of dexamethasone MCs) through SC injection and eye drops in the phacoemulsification combined with intraocular lens implantation (Phaco-IOL) rabbit model. In Phaco-IOL rabbit eyes, a single SC injection of SKD MCs (0.4 mg dexamethasone equiv.) showed anti-inflammatory effects comparable to Maxidex eye drops and completely alleviated the inflammation within 28 days, while an SC injection of Maxidex at the same dose only provided anti-inflammatory effects for 7 days. The study on the dose-dependent anti-inflammatory effects of SKD MCs showed no significant difference in anti-inflammatory effects for the high dosage (0.8 mg dexamethasone equiv.) and the low dosage (0.4 mg dexamethasone equiv.) in 28 days. Nevertheless, systematic drug distribution of SKD MCs and Maxidex in normal rabbits after SC injection demonstrates that the drug concentration in conjunctiva was higher for the high dosage and that a considerable amount of prodrug and dexamethasone could still be detected in the cornea and iris-ciliary body at least 84 days for SKD MCs at high dosage. Furthermore, no persistent elevated intraocular pressure and abnormality in retinal structure and thickness were observed, confirming the excellent safety of long-acting SKD MCs post-SC injection. Our findings provide valuable insights into using prodrug-based MCs for treating ocular postoperative inflammation, and the detailed drug distribution analysis would promote the clinical translation of these MCs in ocular diseases.

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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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