S. Yallappa, Shoriya Aruni Abdul Manaf, Gurumurthy Hegde. Synthesis of a biocompatible nanoporous carbon and its conjugation with florescent dye for cellular imaging and targeted drug delivery to cancer cells. New Carbon Mater., 2018, 33(2): 162-172. doi: 10.1016/S1872-5805(18)60332-4
Citation: S. Yallappa, Shoriya Aruni Abdul Manaf, Gurumurthy Hegde. Synthesis of a biocompatible nanoporous carbon and its conjugation with florescent dye for cellular imaging and targeted drug delivery to cancer cells. New Carbon Mater., 2018, 33(2): 162-172. doi: 10.1016/S1872-5805(18)60332-4

Synthesis of a biocompatible nanoporous carbon and its conjugation with florescent dye for cellular imaging and targeted drug delivery to cancer cells

doi: 10.1016/S1872-5805(18)60332-4
  • Received Date: 2017-12-30
  • Accepted Date: 2018-04-28
  • Rev Recd Date: 2018-04-02
  • Publish Date: 2018-04-28
  • A nanoporous carbon (NPC) was synthesized from Oil palm leaves (OPL) by pyrolysis at 600℃ in a N2 atmosphere, oxidized by a mixture of sulfuric and nitric acids (3:1 vol/vol) and conjugated with coumarin-6 as a fluorescence dye for cellular imaging and drug delivery to cancer cells. The structure, morphology and dispersion stability of NPC in aqueous media before and after the conjugation were investigated by XRD, FT-IR, Raman spectroscopy, SEM, TEM and zeta potential measurement. Cell uptake for the conjugated NPC was investigated by fluorescence microscopy. Results indicate that the cellulose, hemicelluloses and lignin in OPL convert to a graphitic structure by pyrolysis. NPC consists of spherical nanoparticles with diameters of 30-50 nm and has a high graphitic content with an ID/IG ratio of 0.7. The coumarin-6 is successfully conjugated to NPC by forming a complex. Both NPC and the conjugated NPC have a high dispersion stability in aqueous media. NPC is biocompatible with a negligible cytotoxicity. The conjugated NPC exhibits a high cell uptake, is highly biocompatible for normal cells and toxic for tested human cancer cells. NPC is a good candidate for cellular imaging and targeted drug delivery.
  • loading
  • Matsumura Y, Maeda H. A new concept for macromolecular therapeutics in cancer chemotherapy:mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs[J]. Cancer Res, 1986, 46:6387-92.
    Jain R K. Delivery of molecular and cellular medicine to solid tumors[J]. Adv Drug Deliv Rev, 2001, 46:149-68.
    Mickler F M, M ckl L, Ruthardt N, et al. Tuning nanoparticle uptake:live-cell imaging reveals two distinct endocytosis mechanisms mediated by natural and artificial EGFR targeting ligand[J]. Nano Lett, 2012, 12:3417-23.
    Liu Y, Lu W. Recent advances in brain tumor-targeted nano-drug delivery systems[J]. Expert Opin Drug Deliv, 2012, 9:671-86.
    Ashley C E, Carnes E C, Phillips G K, et al. The targeted delivery of multicomponent cargos to cancer cells by nanoporous particle-supported lipid bilayers[J]. Nat Mater, 2011, 10:389-97.
    Florence AT. Targeting nanoparticles:the constraints of physical laws and physical barriers[J]. J Control Release, 2012, 164:115-24.
    Agarwal S, Sane R, Oberoi R, et al. Delivery of molecularly targeted therapy to malignant glioma, a disease of the whole brain[J]. Expert Rev Mol Med, 2011, 13:17.
    Brown SD, Nativo P, Smith Jo-Ann, et al. Gold nanoparticles for the improved anticancer drug delivery of the active component of oxaliplatin[J]. J Am Chem Soc, 2010, 132:4678-84.
    Yallappa S, Manjanna J, Dhananjaya BL, et al. Phytosynthesis of gold nanoparticles using Mappia foetida leaves extract and their conjugation with folic acid for delivery of doxorubicin to cancer cells[J]. J Mater Sci:Mater Med, 2015, 26:235-47.
    Barbe C, Bartlett J, Kong L, et al. Silica particles:A novel drug-delivery system[J]. Adv Mater, 2004, 16:1959-66.
    Kunal B, Sourav P M, Audrey G, et al. Biological interactions of carbon-based nanomaterials:From coronation to degradation[J]. Nanomedicine, 2016, 12(2):333-351.
    Feng Y, Lee K, farhat H, et al. Current ON/OF ration enhancement of FETs with bundled CNTs[J]. J Appl Phys, 2009, 106(10):104505-09.
    Chun X G, Jiale X, Bin W, et al. A new class of fluorescent-dots:long luminescent lifetime bio-dots self-assembled from DNA at low temperatures[J]. Sci Rep, 2013, 3, 2957:1-6.
    Mou X, Ali Z, Li S, et al. Applications of magnetic nanoparticles in targeted drug delivery system[J]. J Nanosci Nanotechnol, 2015, 15(1):54-62.
    Xiao K, Luo J, Li Y, et al. PEG-oligocholic acid telodendrimer micelles for the targeted delivery of doxorubicin to B-cell lymphoma[J]. J Controlled Release, 2011, 155:272-81.
    Jaeyun K, Lan C, Dmitry S, et al.Targeted delivery of nanoparticles to ischemic muscle for imaging and therapeutic angiogenesis[J]. Nano Lett, 2011, 11:694-700.
    Cheng Z 1, Al Zaki A, Hui J Z, et al. Multifunctional nanoparticles:cost versus benefit of adding targeting and imaging capabilities[J]. Science, 2012, 338:903-10.
    Yu C, Hangrong C, Deping Z, et al. Core/shell structured hollow mesoporous nanocapsules:a potential platform for simultaneous cell imaging and anticancer drug delivery[J]. ACS Nano, 2010, 4:6001-13.
    Shihui W, Hui L, Hongdong C, et al. Drug delivery:targeted and pH-responsive delivery of doxorubicin to cancer cells using multifunctional dendrimer-modified multi-walled carbon nanotubes[J]. Adv Healthcare mater, 2013, 2:1267-76.
    Xinxing M, Huiquan T, Kai Y, et al. A functionalized graphene oxide-iron oxide nanocomposite for magnetically targeted drug delivery, photothermal therapy, and magnetic resonance imaging[J]. Nano Res, 2012, 5:199-212.
    Nanda G S, Hongqian B, Yongzheng P, et al. Functionalized carbon nanomaterials as nanocarriers for loading and delivery of a poorly water-soluble anticancer drug:a comparative study[J]. Chem. Commun, 2011, 47:5235-37.
    So Y P, Hyun U L, Eun S P, et al. Photoluminescent green carbon nanodots from food-waste-derived sources:Large-scale synthesis, properties, and biomedical applications[J]. ACS Appl Mater Interfaces, 2014, 6:3365-70.
    Wang L, Sun Q, Wang X, et al. Using hollow carbon nanospheres as a light-induced free radical generator to overcome chemotherapy resistance[J]. J Am Chem Soc, 2015, 137(5):1947-55.
    Zhang X B, Tong H W, Liu S M, et al. An improved St ber method towards uniform and monodisperse Fe3O4@C nanospheres[J]. J Mater Chem A, 2013, 1:7488-93.
    Pol VG, Motiei M, Gedanken A, et al. Carbon spherules:synthesis, properties and mechanistic elucidation[J]. Carbon, 2004, 42:111-116.
    Pei-Ying L, Chiung-Wen H, Mei-Lang K, et al. Eco-friendly synthesis of shrimp egg-derived carbon dots for fluorescent bioimaging[J]. J Biotech, 2014, 189:114-19.
    Daeun K, Yuri C, Eeseul S, et al. Sweet nanodot for biomedical imaging:carbon dot derived from xylitol[J]. RSC Adv, 2014, 4:23210-13.
    Manar SAA, Roy P, Sharma K V, et al. Catalyst-free synthesis of carbon nanospheres for potential biomedical applications:waste to wealth approach[J]. RSC Adv, 2015, 5:24528-33.
    Rafatullah M, Ahmad T, Ghazali A, et al. Oil palm biomass as a precursor of activated carbons:a review[J]. Crit Rev Environ Sci Technol, 2013, 43(11):1117-61.
    Hashim R, Nadhari WNAW, Sulaiman O, et al. Characterization of raw materials and manufactured binderless particles board from oil palm biomass[J]. Mater Des, 2011, 32:246-254.
    Wang J T, Chen C, Wang E, et al. A new carbon allotrope with six-fold helical chain in all sp2 bonding networks[J]. Sci Rep, 2014, 4:4339-44.
    Krishnamurthy G, Namitha R. Synthesis of structurally novel carbon micro/nanospheres by low temperature-hydrothermal process[J]. J Chil Chem Soc, 2013, 58(3):1930-33.
    Panagiotis T, Thomas F F, Peter S. Carbon as catalyst and support for electrochemical energy conversion[J]. Carbon, 2014, 75:5-42.
    Galeener F L, Sen P N. Molecular-dynamics study of a three-dimensional one-component model for distortive phase transitions[J]. Phys Rev B, 1978, 17:1928.
    Hussain N, Jaitley V, Florence AT. Recent advances in the understanding of uptake of microparticulates across the gastrointestinal lymphatics[J]. Adv Drug Deliv Rev, 2001, 50:107-42.
    Choi C H, Alabi C A, Webster P, et al. Mechanism of active targeting in solid tumors with transferrin-containing gold nanoparticles[J]. Proc Natl Acad Sci USA, 2010, 107:1235-40.
    Kirpotin D B, Drummond D C, Shao Y, et al. Antibody targeting of long-circulating lipidic nanoparticles does not increase tumor localization but does increase internalization in animal models[J]. Cancer Res, 2006, 66:6732-40.
    Hyun U L, So Y P, Eun S P, et al. Photoluminescent carbon nanotags from harmful cyanobacteria for drug delivery and imaging in cancer cells[J]. Sci Rep, 2014, 4:4665-72.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(1)

    Article Metrics

    Article Views(349) PDF Downloads(249) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return