[1] MÁRMOL I, SÁNCHEZ-DE-DIEGO C, PRADILLA DIESTE A, et al. Colorectal carcinoma: a general overview and future perspectives in colorectal cancer[J]. Int J Mol Sci, 2017, 18(1):197. doi:  10.3390/ijms18010197
[2] DEKKER E, TANIS P J, VLEUGELS J L A, et al. Colorectal cancer[J]. Lancet, 2019, 394(10207):1467-1480. doi:  10.1016/S0140-6736(19)32319-0
[3] ATTOUB S, ARAFAT K, KHALAF T, et al. Frondoside A enhances the anti-cancer effects of oxaliplatin and 5-fluorouracil on colon cancer cells[J]. Nutrients, 2018, 10(5):560. doi:  10.3390/nu10050560
[4] FUJIE Y, YAMAMOTO H, NGAN C Y, et al. Oxaliplatin, a potent inhibitor of survivin, enhances paclitaxel-induced apoptosis and mitotic catastrophe in colon cancer cells[J]. Jpn J Clin Oncol, 2005, 35(8):453-463. doi:  10.1093/jjco/hyi130
[5] OHISHI T, KANEKO M K, YOSHIDA Y, et al. Current targeted therapy for metastatic colorectal cancer[J]. Int J Mol Sci, 2023, 24(2):1702. doi:  10.3390/ijms24021702
[6] 陈炳辰, 于恩达. 增强紫杉醇对结直肠癌化疗疗效的研究进展[J]. 药学实践杂志, 2020, 38(6):501-505.
[7]

MARUPUDI N I, HAN J E, LI K W, et al. Paclitaxel: a review of adverse toxicities and novel delivery strategies[J]. Expert Opin Drug Saf, 2007, 6(5):609-621. doi:  10.1517/14740338.6.5.609
[8]

ALQAHTANI F Y, ALEANIZY F S, EL TAHIR E, et al. Paclitaxel[J]. Profiles Drug Subst Excip Relat Methodol, 2019, 44:205-238.
[9]

LILENBAUM R C, RATAIN M J, MILLER A A, et al. Phase I study of paclitaxel and topotecan in patients with advanced tumors: a cancer and leukemia group B study[J]. J Clin Oncol, 1995, 13(9):2230-2237. doi:  10.1200/JCO.1995.13.9.2230
[10]

BEKAII-SAAB T S, RODA J M, GUENTERBERG K D, et al. A phase I trial of paclitaxel and trastuzumab in combination with interleukin-12 in patients with HER2/neu-expressing malignancies[J]. Mol Cancer Ther, 2009, 8(11):2983-2991. doi:  10.1158/1535-7163.MCT-09-0820
[11]

HU T, TO K K, WANG L, et al. Reversal of P-glycoprotein(P-gp)mediated multidrug resistance in colon cancer cells by cryptotanshinone and dihydrotanshinone of Salvia miltiorrhiza[J]. Phytomedicine, 2014, 21(11):1264-1272. doi:  10.1016/j.phymed.2014.06.013
[12]

YANG C P H, HORWITZ S B. Taxol®: the first microtubule stabilizing agent[J]. Int J Mol Sci, 2017, 18(8):1733. doi:  10.3390/ijms18081733
[13]

ZHU L Y, CHEN L Q. Progress in research on paclitaxel and tumor immunotherapy[J]. Cell Mol Biol Lett, 2019, 24:40. doi:  10.1186/s11658-019-0164-y
[14]

WANG X T, ZHANG C N, BAO N. Molecular mechanism of palmitic acid and its derivatives in tumor progression[J]. Front Oncol, 2023, 13:1224125. doi:  10.3389/fonc.2023.1224125
[15]

FHU C W, ALI A. Fatty acid synthase: an emerging target in cancer[J]. Molecules, 2020, 25(17):3935. doi:  10.3390/molecules25173935
[16] 韦武豪, 陈新美, 陈建明, 等. 紫杉醇饱和脂肪酸酯脂质体的药效学及组织分布研究[J]. 中国新药杂志, 2023, 32(7):728-734. doi:  10.3969/j.issn.1003-3734.2023.07.012
[17]

KAN P, TSAO C W, WANG A J, et al. A liposomal formulation able to incorporate a high content of Paclitaxel and exert promising anticancer effect[J]. J Drug Deliv, 2011, 2011:629234.
[18]

NGUYEN A, CHAO P H, ONG C Y, et al. Chemically engineering the drug release rate of a PEG-paclitaxel conjugate using click and steric hindrance chemistries for optimal efficacy[J]. Biomaterials, 2022, 289:121735. doi:  10.1016/j.biomaterials.2022.121735
[19]

WU J. The enhanced permeability and retention(EPR)effect: the significance of the concept and methods to enhance its application[J]. J Pers Med, 2021, 11(8):771. doi:  10.3390/jpm11080771
[20] 陈炳辰. 紫杉醇棕榈酸酯纳米给药系统的构建及抗结直肠癌作用研究[D]. 海军军医大学, 2021.
[21]

HU Y J, GU C C, WANG X F, et al. Asymmetric total synthesis of taxol[J]. J Am Chem Soc, 2021, 143(42):17862-17870. doi:  10.1021/jacs.1c09637
[22]

XU M Q, HAO Y L, WANG J R, et al. Antitumor Activity of α-Linolenic Acid-Paclitaxel Conjugate Nanoparticles: in vitro and in vivo[J]. Int J Nanomedicine, 2021, 16:7269-7281. doi:  10.2147/IJN.S331578
[23] 余侬, 陈建明. HPLC法同时测定大鼠血浆中紫杉醇棕榈酸酯及其活性代谢产物紫杉醇的含量[J]. 海峡药学, 2016, 28(5):23-25. doi:  10.3969/j.issn.1006-3765.2016.05.010
[24] 程丹, 余侬, 许幼发, 等. 紫杉醇棕榈酸酯脂质体的制备及初步药效学和安全性评价[J]. 中国药学杂志, 2018, 53(8):614-619. doi:  10.11669/cpj.2018.08.010
[25]

PENOY N, GRIGNARD B, EVRARD B, et al. A supercritical fluid technology for liposome production and comparison with the film hydration method[J]. Int J Pharm, 2021, 592:120093. doi:  10.1016/j.ijpharm.2020.120093
[26]

NAJLAH M, HIDAYAT K, OMER H K, et al. A facile approach to manufacturing non-ionic surfactant nanodipsersions using proniosome technology and high-pressure homogenization[J]. J Liposome Res, 2015, 25(1):32-37. doi:  10.3109/08982104.2014.924140
[27]

SHAH V M, NGUYEN D X, PATEL P, et al. Liposomes produced by microfluidics and extrusion: a comparison for scale-up purposes[J]. Nanomed-Nanotechnol Biol Med, 2019, 18:146-156. doi:  10.1016/j.nano.2019.02.019