Prolonged activity of a recombinant manganese superoxide dismutase through a formulation of polymeric multi-layer nanoassemblies targeting cancer cells

被引:2
作者
Russo, Giacomo [1 ]
Iaccarino, Giulia [2 ]
Piccolo, Marialuisa [3 ]
Ferraro, Maria Grazia [3 ]
Vecchione, Raffaele [2 ]
Grumetto, Lucia [4 ,5 ]
Netti, Paolo A. [2 ]
Santamaria, Rita [3 ,5 ]
机构
[1] Edinburgh Napier Univ, Sch Appl Sci, Sighthill Campus,9 Sighthill Ct, Edinburgh EH11 4BN, Midlothian, Scotland
[2] Ist Italian Tecnol, Ctr Adv Biomat Hlth Care CRIB, Largo Barsanti & Matteucci 53, I-80125 Naples, Italy
[3] Univ Naples Federico II, Sch Med & Surg, Dept Pharm, Biochem Lab, Via D Montesano 49, I-80131 Naples, Italy
[4] Univ Naples Federico II, Sch Med & Surg, Dept Pharm, Pharm Anal & Biopharm Lab, Via D Montesano 49, I-80131 Naples, Italy
[5] Consorzio Interuniv INBB, Viale Medaglie dOro 305, I-00136 Rome, Italy
关键词
Superoxide dismutase; Cancer cells; Antiproliferative effect; Protein stability; Nanocarrier; Layer-by-layer deposition; Nanofabrication; OVARIAN-CANCER; MNSOD; CISPLATIN;
D O I
10.1016/j.ejps.2021.105825
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new isoform of human manganese superoxide dismutase (SOD) has been recently isolated and obtained in a synthetic recombinant form and termed rMnSOD. As compared to other SODs, this isoform exhibits a dramatically improved cellular uptake and an intense antioxidant and antitumoral activity. Unfortunately, its use is severely hampered as this active pharmaceutical ingredient (API) in solution suffers from remarkable instability, which realizes as an interplay of unfolding and aggregation phenomena. This leads the API to be ineffective after three weeks only when stored at 4 degrees C. A formulation strategy was undertaken to mitigate this instability. This was based on the incorporation of the API in hyaluronic acid and its layer-by-layer deposition over a chitosan-n-acetyl cysteine- monolayer nanoemulsion (NE) and its subsequent coverage with a further external interface of a chitosan-n-acetyl cysteine. The obtained constructs were tested over a selected panel of healthy and cancerous cell lines. The undertaken formulation strategy enhanced the API's effect in vitro already at time zero, maintaining the efficacy of this anticancer agent until up to 30 weeks when stored at 4 degrees C.
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页数:10
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