Self-Assembled Silk Fibroin-Based Aggregates for Delivery of Camptothecin

Abstract

A water-soluble hydrolysate of silk fibroin (SF) (~30 kDa) was esterified with tocopherol, ergocalciferol, and testosterone to form SF aggregates for the controlled delivery of the anticancer drug camptothecin (CPT). Elemental analysis and 1H NMR spectroscopy showed a degree of substitution (DS) on SF of 0.4 to 3.8 mol %. Yields of 58 to 71% on vitamins- and testosterone-grafted SF conjugates were achieved. CPT was efficiently incorporated into the lipophilic core of SF aggregates using a dialysis–precipitation method, achieving drug contents of 6.3–8.5 wt %. FTIR spectra and DSC thermograms showed that tocopherol- and testosterone-grafted SF conjugates predominantly adopted a β-sheet conformation. After the esterification of tyrosine residues on SF chains with the vitamin or testosterone, the hydrodynamic diameters almost doubled or tripled that of SF. The zeta potential values after esterification increased to about −30 mV, which favors the stability of aggregates in aqueous medium. Controlled and almost quantitative release of CPT was achieved after 6 days in PBS at 37 °C, with almost linear release during the first 8 h. MCF-7 cancer cells exhibited good uptake of CPT-loaded SF aggregates after 6 h, causing cell death and cell cycle arrest in the G2/M phase. Substantial uptake of the CPT-loaded aggregates into MCF-7 spheroids was shown after 3 days. Furthermore, all CPT-loaded SF aggregates demonstrated superior toxicity to MCF-7 spheroids compared with parent CPT. Blank SF aggregates induced no hemolysis at pH 6.2 and 7.4, while CPT-loaded SF aggregates provoked hemolysis at pH 6.2 but not at pH 7.4. In contrast, parent CPT caused hemolysis at both pH tested. Therefore, CPT-loaded SF aggregates are promising candidates for chemotherapy.

Biomaterials and Extracellular Vesicle Delivery: Current Status, Applications and Challenges

“…Anti-proliferative [ 68 ], anti-inflammatory [ 69 , 70 ], anabolic [ 70 ], and anti-retroviral drugs [ 71 ] have been delivered using silk fibroin. Additional drugs include anti-inflammatory compounds such as curcumin [ 72 , 73 ] and chemotherapeutics [ 74 , 75 ]. Aside from drug delivery, SF has been utilized for the delivery of antibodies [ 76 ], proteins [ 76 , 77 ], hormones (e.g., insulin) [ 78 ], genetic material [ 79 ], and cells (e.g., mesenchymal stem cells) [ 80 ].…”