2019
DOI: 10.1016/j.colsurfb.2019.05.047
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Loading Auristatin PE onto boron nitride nanotubes and their effects on the apoptosis of Hep G2 cells

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Cited by 7 publications
(9 citation statements)
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“…CNTs and BNNTs were extensively explored for biological purposes, including their potential application to hydrophobic drug carrier carriers [14][15][16]. Due to their available hydrophobic inner space, ability to disperse in aqueous solution in the presence or absence or dispersants, and large aspect ratio, both CNTs and BNNTs can either be endocytosed or directly penetrate cell membranes, allowing targeted delivery of hydrophobic drugs.…”
Section: Introductionmentioning
confidence: 99%
“…CNTs and BNNTs were extensively explored for biological purposes, including their potential application to hydrophobic drug carrier carriers [14][15][16]. Due to their available hydrophobic inner space, ability to disperse in aqueous solution in the presence or absence or dispersants, and large aspect ratio, both CNTs and BNNTs can either be endocytosed or directly penetrate cell membranes, allowing targeted delivery of hydrophobic drugs.…”
Section: Introductionmentioning
confidence: 99%
“…[ 63 ] Through morphological controls and surface modifications, BN nanomaterials could be used as an effective carrier of doxorubicin and realized much enhanced intracellular drug delivery to LNCap prostate cancer cells, [ 35 ] or load Auristatin PE to trigger the mitochondrial‐mediated apoptosis of Hep G2 cells. [ 64 ] Surface chemical modifications of BN nanomaterials could further enhance the specific targeting performances by ligand‐receptor recognitions and promote the therapeutic efficacy. [ 43 , 65 ] Recent advances suggested that hollow BN nanospheres could slowly and endurably release water‐soluble B compounds, which were found to efficiently inhibit LNCap prostate cancer cell growth.…”
Section: Resultsmentioning
confidence: 99%
“…Li et al [28] Solid-state reaction PE-loaded BNNTs 0-100 µg•mL The results indicated that the biodegradation amount of the scaffolds was slower with the incorporation of BNNTs. The SEM and fluorescence microscopy images showed that the BNNTs positively impacted cell adhesion and proliferation.…”
Section: Study Selectionmentioning
confidence: 99%
“…The most dominant cell types used in the included articles were human embryonic kidney cells (HEK293, HEK293T) [24,25,74,81,154], human neuroblastoma cells (SH-SY5Y) [30,64,68,73,76,79,82,155], mouse embryonic fibroblasts (NIH/3T3) [70], human dermal fibroblasts (HDF) [31,36,48,51,55], lung fibroblasts (MRC-5) [65,156], dental pulp fibroblasts [34,41,62], lung epithelium cells (A549) [37,55,74], macrophage cells (RAW 264.7) [49,74], human liver epithelium (HeP G2) [27,28,37], human peripheral blood (NB4) [37], glioblastoma cells (malignant U87 [30,37,156], T98 [80,156]), mammary gland adenocarcinoma cells (MCF-7) [156], N9 murine microglia cells [50], osteoblasts [54,66,75,77], osteoblast precursor cell line derived from mouse musculus calvaria (M3CT3) [47]<...…”
Section: Cell Sourcesmentioning
confidence: 99%
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