2022
DOI: 10.1016/j.ijbiomac.2021.12.189
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Fabrication of cellulose nanocrystals as potential anticancer drug delivery systems for colorectal cancer treatment

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Cited by 28 publications
(13 citation statements)
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“…As a result of their features, NCs in the bloodstream are passively targeted to organs that are rich in mononuclear phagocytic system (MPS) cells, e.g., liver, spleen, and lung. 302,303 Furthermore, NCs can also serve as carriers for smallmolecular drugs if they are used with protein−drug complexes as stabilizers. Xin et al reported an NC-based nanoplatform with dual loading of paclitaxel and marimastat for efficient treatment of metastatic cancer.…”
Section: Inorganic Nddss In Cancer Therapymentioning
confidence: 99%
See 1 more Smart Citation
“…As a result of their features, NCs in the bloodstream are passively targeted to organs that are rich in mononuclear phagocytic system (MPS) cells, e.g., liver, spleen, and lung. 302,303 Furthermore, NCs can also serve as carriers for smallmolecular drugs if they are used with protein−drug complexes as stabilizers. Xin et al reported an NC-based nanoplatform with dual loading of paclitaxel and marimastat for efficient treatment of metastatic cancer.…”
Section: Inorganic Nddss In Cancer Therapymentioning
confidence: 99%
“…NCs have high drug loading capacity, platform stability, ease of scaling up, and good water solubility. As a result of their features, NCs in the bloodstream are passively targeted to organs that are rich in mononuclear phagocytic system (MPS) cells, e.g., liver, spleen, and lung. , …”
Section: Inorganic Nddss In Cancer Therapymentioning
confidence: 99%
“…80 There were signs of aggregation and the formation of strong hydrogen bonds between the hydroxyl groups on the surfaces of cellulose chains during the sample preparation and drying procedures. 81 Furthermore, a slight aggregation could be induced across the CNCs by the freeze drying process. 82 According to Vadim G. Kessler et al ., spherically shaped CNCs can be used for carrying drugs with a long-term drug release and the maintenance of antibacterial properties.…”
Section: Resultsmentioning
confidence: 99%
“…The whole assembly was maintained on a magnetic stirrer at 600 rpm for a period of 600 min, and samples were withdrawn at an interval of 1 h for 8 h and replaced with an equal volume of buffer. Samples were appropriately diluted with buffer and analysed for the drug (β-sitosterol) using a UV spectrophotometer at 279 nm [ 37 , 38 ].…”
Section: Methodsmentioning
confidence: 99%