Targeting efficacy and anticancer activity of polymeric nanoparticles of SN-38 on colon cancer cell lines

被引:3
|
作者
Prasad, Shilpi [1 ]
Dangi, J. S. [2 ]
机构
[1] Siddhi Vinayaka Inst Technol & Sci, Dept Pharmaceut, Bilaspur 495001, Chhattisgarh, India
[2] SLT Inst Pharmaceut Sci, Dept Pharmaceut, GGV, Bilaspur, CG, India
关键词
Polymeric nanoparticles; Colorectal cancer; Cell line; Gamma Scintigraphy; Colon targeting; Camptothecin; LIPOSOME-BASED FORMULATION; IN-VITRO; METABOLITE SN-38; DELIVERY-SYSTEM; IRINOTECAN; BIODISTRIBUTION; CPT-11; STABILITY; ASSAY; VIVO;
D O I
10.1186/s43094-023-00462-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundColorectal cancer is the third most prevailing cancer in the whole world. Chemotherapeutic agents which are used for treatment have severe side effects and also have unwanted exposure to healthy cells. In the present study, polymeric nanoparticles of SN-38 were prepared (using cationic and anionic polymers). They were optimized by Box Behnken design and characterized for its physicochemical properties and in vitro drug release. Optimized formulation (CsENP) was evaluated for its targeting efficacy by Gamma Scintigraphy studies on Swiss Albino mice and in vitro Cytotoxic assay against colon cancer cell line, viz. HT-29.ResultsThe images of Whole body gamma scintigraphy imaging of Swiss Albino mice show that CsENP remained intact till 2 h and after that at 4 h imaging it started dispersing and releasing drug which continued till 20 h. In Organ distribution studies, no radioactivity was traced in heart from the formulation. Even in liver, spleen, kidney and lung trace radioactivity was seen after 6 h. In case of CsENP radioactivity was seen in small intestine after 2 h and maximum (87.8% radioactivity) is seen in colon and rectum area after 4 h. At equivalent concentrations, the in vitro cell viability of HT-29 cells after 72 h incubation time showed that CsENP have enhanced cytotoxicity.ConclusionsThe results obtained of Whole body gamma scintigraphy imaging and organ distribution of Swiss Albino mice show that CsENP is Colon targeting and was found to be effective against colon cancer cell lines.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Cell diameter measurements obtained with a handheld cell counter could be used as a surrogate marker of G2/M arrest and apoptosis in colon cancer cell lines exposed to SN-38
    Tahara, Makiko
    Inoue, Takeshi
    Miyakura, Yasuyuki
    Horie, Hisanaga
    Yasuda, Yoshikazu
    Fujii, Hirofumi
    Kotake, Kenjiro
    Sugano, Kokichi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 434 (04) : 753 - 759
  • [42] Short hairpin RNAs targeting Bcl-xL modulate senescence and apoptosis following SN-38 and irinotecan exposure in a colon cancer model
    Guichard, S. M.
    Hua, M. L.
    Kang, P.
    Macpherson, J. S.
    Jodrell, D. I.
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2007, 60 (05) : 651 - 660
  • [43] Short hairpin RNAs targeting Bcl-xL modulate senescence and apoptosis following SN-38 and irinotecan exposure in a colon cancer model
    S. M. Guichard
    M. L. Hua
    P. Kang
    J. S. Macpherson
    D. I. Jodrell
    Cancer Chemotherapy and Pharmacology, 2007, 60 : 651 - 660
  • [44] Combination of SN-38 with gefitinib or imatinib overcomes SN-38-resistant small-cell lung cancer cells
    Takigawa, Nagio
    Takeyama, Masami
    Kozuki, Toshiyuki
    Shibayama, Takuo
    Hisamoto, Akiko
    Kiura, Katsuyuki
    Tada, Atsuhiko
    Hotta, Katsuyuki
    Umemura, Shigeki
    Ohashi, Kadoaki
    Fujiwara, Yoshiro
    Takata, Saburo
    Ichihara, Eiki
    Osawa, Masahiro
    Tabata, Masahiro
    Tanimoto, Mitsune
    Takahashi, Kiyoshi
    ONCOLOGY REPORTS, 2007, 17 (05) : 983 - 987
  • [45] Targeting Colorectal Cancer Stem-Like Cells with Anti-CD133 Antibody-Conjugated SN-38 Nanoparticles
    Ning, Sin-Tzu
    Lee, Shin-Yu
    Wei, Ming-Feng
    Peng, Cheng-Liang
    Lin, Susan Yun-Fan
    Tsai, Ming-Hsien
    Lee, Pei-Chi
    Shih, Ying-Hsia
    Lin, Chun-Yen
    Luo, Tsai-Yueh
    Shieh, Ming-Jium
    ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (28) : 17793 - 17804
  • [46] Choline kinase inhibition with flavopiridol enhances SN-38 induced apoptosis in human colon cancer cells
    Kennealey, PT
    Racanelli, A
    Motwani, M
    Hendrix, PJ
    Jacobi, R
    Korytowsky, B
    Chen, JH
    Schwartz, G
    Singer, S
    JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2003, 197 (03) : S75 - S75
  • [47] Biosynthesis and characterization of copper oxide nanoparticles and its anticancer activity on human colon cancer cell lines (HCT-116)
    Gnanavel, V.
    Palanichamy, V.
    Roopan, Selvaraj Mohana
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2017, 171 : 133 - 138
  • [48] The effect of SN-38 on cell proliferation and on production of urokinase-type plasminogen activator and its inhibitor in human lung cancer cell lines
    Ishikawa, H
    Satoh, H
    Kamma, H
    Naito, T
    Ohtsuka, M
    Ogata, T
    Hasegawa, S
    CANCER RESEARCH THERAPY & CONTROL, 1998, 5 (02): : 97 - 105
  • [49] Comparison, synthesis and evaluation of anticancer drug-loaded polymeric nanoparticles on breast cancer cell lines
    Eatemadi, Ali
    Darabi, Masoud
    Afraidooni, Loghman
    Zarghami, Nosratollah
    Daraee, Hadis
    Eskandari, Leila
    Mellatyar, Hassan
    Abolfazl, Akbarzadeh
    ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2016, 44 (03) : 1008 - 1017
  • [50] SN-38 active loading in poly(lactic-co-glycolic acid) nanoparticles and assessment of their anticancer properties on COLO-205 human colon adenocarcinoma cells
    Essa, Sherief
    Daoud, Jamal
    Lafleur, Michel
    Martel, Sylvain
    Tabrizian, Maryam
    JOURNAL OF MICROENCAPSULATION, 2015, 32 (08) : 784 - 793