| Literature DB >> 32980548 |
Zhifeng Zhao1, Zhenshan Jia1, Kirk W Foster2, Xin Wei1, Fangfang Qiao1, Haochen Jiang1, Yan Jin1, Guojuan Li1, Ningrong Chen1, Gang Zhao1, Geoffrey M Thiele3, Jennifer L Medlin4, James R O'Dell3, Dong Wang5.
Abstract
Lupus nephritis (LN) is a major cause of morbidity and mortality among systemic lupus erythematosus patients. Glucocorticoids (GCs) are uniformly used in clinical LN management. Their notorious toxicities, however, have hampered the long-term clinical application. To circumvent GC side effects while maintaining their potent therapeutic efficacy, we have developed a macromolecular prodrug nanomedicine based on dexamethasone (ZSJ-0228). The focus of this study was to investigate its long-term efficacy and, most importantly, safety in the lupus-prone NZB/W F1 mouse. Monthly ZSJ-0228 treatment for five months significantly reduced the incidence of nephritis in NZB/W F1 mice with an improved survival rate. In contrast to treatment with dose equivalent daily free dexamethasone, long-term monthly ZSJ-0228 did not result in any measurable GC-associated side effects. With its outstanding efficacy and exceptional safety, it is anticipated that ZSJ-0228 may be a novel therapy for long-term clinical management of LN.Entities:
Keywords: Dexamethasone; Lupus nephritis; Nanomedicine; Prodrug; Side effects; ZSJ-0228
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Year: 2020 PMID: 32980548 PMCID: PMC7736168 DOI: 10.1016/j.nano.2020.102302
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307