A Theranostic Cellulose Nanocrystal‐Based Drug Delivery System with Enhanced Retention in Pulmonary Metastasis of Melanoma. Issue 18 (18th March 2021)

• Record Type: Journal Article
• Authors: Imlimthan, Surachet; Khng, You Cheng; Keinänen, Outi; Zhang, Wenzhong; Airaksinen, Anu J.; Kostiainen, Mauri A.; Zeglis, Brian M.; Santos, Hélder A.; Sarparanta, Mirkka
• Is Part Of: Small. Volume 17:Issue 18(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-03-18
• Subjects: cellulose nanocrystal -- drug delivery system -- Lutetium‐177 -- metastatic melanoma -- theranostic nanosystem -- vemurafenib; Nanotechnology -- Periodicals; Nanoparticles -- Periodicals; Microtechnology -- Periodicals; 620.5
• DOI: 10.1002/smll.202007705
• Languages: English
• ISSNs: 1613-6810

Abstract

Abstract: Metastatic melanoma can be difficult to detect until at the advanced state that decreases the survival rate of patients. Several FDA‐approved BRAF inhibitors have been used for treatment of metastatic melanoma, but overall therapeutic efficacy has been limited. Lutetium‐177 ( 177 Lu) enables simultaneous tracking of tracer accumulation with single‐photon emission computed tomography and radiotherapy. Therefore, the codelivery of 177 Lu alongside chemotherapeutic agents using nanoparticles (NPs) might improve the therapeutic outcome in metastatic melanoma. Cellulose nanocrystals (CNC NPs) can particularly deliver payloads to lung capillaries in vivo. Herein, 177 Lu‐labeled CNC NPs loaded with vemurafenib ([ 177 Lu]Lu‐CNC‐V NPs) is developed and the therapeutic effect in BRAF V600E mutation‐harboring YUMM1.G1 murine model of lung metastatic melanoma is investigated. The [ 177 Lu]Lu‐CNC‐V NPs demonstrate favorable radiolabel stability, drug release profile, cellular uptake, and cell growth inhibition in vitro. In vivo biodistribution reveals significant retention of the [ 177 Lu]Lu‐CNC‐V NPs in the lung, liver, and spleen. Ultimately, the median survival time of animals is doubly increased after treatment with [ 177 Lu]Lu‐CNC‐V NPs compared to control groups. The enhanced therapeutic efficacy of [ 177 Lu]Lu‐CNC‐V NPs in the lung metastatic melanoma animal model provides convincing evidence for the potential of clinical translation for theranostic CNC NP‐based drug delivery systems after intravenous administration. Abstract : This study describes theranostic cellulose nanocrystals ([ 177 Lu]Lu‐cellulose nanocrystals (CNC)‐V nanoparticles (NPs)) for the codelivery of BRAF inhibitor vemurafenib and the radioisotope lutetium‐177 for chemotherapy and radiotherapy of pulmonary metastases of melanoma through enhanced retention in the lung. The [ 177 Lu]Lu‐CNC‐V NPs prolong the survival of syngeneic YUMM1.G1 melanoma tumor‐bearing mice and decrease the tumor burden in the lung over either vemurafenib or radiotherapy alone.