journal article·2023-09

From phytomedicine to photomedicine: quercetin-derived carbon nanodots—synthesis, characterization and healthcare applications

Gaurav Gopal Naik, Ravi Pratap, Debadatta Mohapatra, Singh Shreya, Deepak K. Sharma, Avanish S. Parmar, Arjun Patra, Alakh N Sahu

Journal of Materials Science· Volume 58· Issue 34
Publisher page

Abstract

No abstract is available for this record. The assistant can identify its topic from the title, but cannot infer the study’s results.

Source: Not provided · Quality: missing

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Heavy Metal Exposure and Toxicity · Graphene and Nanomaterials Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (58)

Show source-provided references
1. Marin R, Benayas A, García-Carillo N et al (2022) Nanoprobes for biomedical imaging with tunable near-infrared optical properties obtained via green synthesis. Adv Photon Res 3:2100260–2100270. https://doi.org/10.1002/adpr.20210026010.1002/adpr.202100260 ↗
2. Su L, Qin S, Cai Y et al (2022) Co, N-doped carbon dot nanozymes with acid pH-independence and substrate selectivity for biosensing and bioimaging. Sens Actuators B: Chem 353:131150–131155. https://doi.org/10.1016/j.snb.2021.13115010.1016/j.snb.2021.131150 ↗
3. Naik GG, Minocha T, Verma A et al (2022) Asparagus racemosus root-derived carbon nanodots as a nano-probe for biomedical applications. J Mater Sci 57:20380–20401. https://doi.org/10.1007/s10853-022-07908-z10.1007/s10853-022-07908-z ↗
4. Naik GG, Alam MB, Pandey V et al (2020) Pink fluorescent carbon dots derived from the phytomedicine for breast cancer cell imaging. ChemistrySelect 5(23):6954–696010.1002/slct.202001613 ↗
5. Naik GG, Shah J, Balasubramaniam AK, Sahu AN (2021) Applications of natural product-derived carbon dots in cancer biology. Nanomedicine 16:587–608. https://doi.org/10.2217/nnm-2020-042410.2217/nnm-2020-0424 ↗
6. Wang B, Song H, Qu X et al (2021) Carbon dots as a new class of nanomedicines: opportunities and challenges. Coord Chem Rev 442:214010–214025. https://doi.org/10.1016/j.ccr.2021.21401010.1016/j.ccr.2021.214010 ↗
7. Design and synthesis of dual-responsive carbon nanodots loaded with cisplatin for targeted therapy of lung cancer therapy and nursing care | SpringerLink. https://link.springer.com/article/https://doi.org/10.1007/s10876-020-01959-5. Accessed 27 Mar 202310.1007/s10876-020-01959-5 ↗
8. John TS, Yadav PK, Kumar D et al (2020) Highly fluorescent carbon dots from wheat bran as a novel drug delivery system for bacterial inhibition. Luminescence 35:913–923. https://doi.org/10.1002/bio.380110.1002/bio.3801 ↗
9. Shen N, Wang T, Gan Q et al (2022) Plant flavonoids: classification, distribution, biosynthesis, and antioxidant activity. Food Chem 383:132531-132539. https://doi.org/10.1016/j.foodchem.2022.13253110.1016/j.foodchem.2022.132531 ↗
10. Huang C, Zhou Y, Yu G et al (2021) Glutathione-functionalized long-period fiber gratings sensor based on surface plasmon resonance for detection of As3+ ions. Nanotechnology. https://doi.org/10.1088/1361-6528/ac1b5610.1088/1361-6528/ac1b56 ↗
11. Mohapatra D, Pratap R, Pandey V et al (2023) Bioengineered dual fluorescent carbon nano dots from Indian long pepper leaves for multifaceted environmental and health utilities. Environ Sci Pollut Res 30:52182–52208. https://doi.org/10.1007/s11356-023-25887-910.1007/s11356-023-25887-9 ↗
12. Aa D, Shegokar R (2016) Polyethylene glycol (PEG): a versatile polymer for pharmaceutical applications. Expert Opin Drug Deliv 13;1257–1275 https://doi.org/10.1080/17425247.118248510.1080/17425247.1182485 ↗
13. Pharmacological effects and safety of Andrographis paniculata (Burm.f.) Nees - Tian - 2022 - Journal of Food Science - Wiley Online Library. https://ift.onlinelibrary.wiley.com/doi/full/https://doi.org/10.1111/1750-3841.16079. Accessed 27 Mar 202310.1111/1750-3841.16079 ↗
14. Tj W (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols : a guide to methods and applications 315–32210.1016/B978-0-12-372180-8.50042-1 ↗
15. Shi N, Sun K, Zhang Z et al (2021) Amino-modified carbon dots as a functional platform for drug delivery: load-release mechanism and cytotoxicity. J Ind Eng Chem 101:372–378. https://doi.org/10.1016/j.jiec.2021.05.04610.1016/j.jiec.2021.05.046 ↗
16. Zhou C, Li H, Liu Y, Wang K (2022) Design and synthesis of dual-responsive carbon nanodots loaded with cisplatin for targeted therapy of lung cancer therapy and nursing care. J Clust Sci 33:331–338. https://doi.org/10.1007/s10876-020-01959-510.1007/s10876-020-01959-5 ↗
17. Borman P, Elder D (2017) Q 2 (R1) Validation of Analytical Procedures: Text and Methodology, ICH quality guidelines: an implementation guide; 127–16610.1002/9781118971147.ch5 ↗
18. Kholiya F, Chatterjee S, Bhojani G et al (2020) Seaweed polysaccharide derived bioaldehyde nanocomposite: potential application in anticancer therapeutics. Carbohydr Polym 240:116282–116291. https://doi.org/10.1016/j.carbpol.2020.11628210.1016/j.carbpol.2020.116282 ↗
19. Souri D, Salimi N, Ghabooli M (2021) Hydrothermal fabrication of pure ZnSe nanocrystals at different microwave irradiation times and their disc-diffusion antibacterial potential against Gram negative bacteria: bio-optical advantages. Inorg Chem Commun 123:108345–108349. https://doi.org/10.1016/j.inoche.2020.10834510.1016/j.inoche.2020.108345 ↗
20. Davin-Regli A, Pagès J-M (2015) Enterobacter aerogenes and Enterobacter cloacae; versatile bacterial pathogens confronting antibiotic treatment. Front Microbiol 6:392–39710.3389/fmicb.2015.00392 ↗
21. Ramírez-Castillo FY, Moreno-Flores AC, Avelar-González FJ et al (2018) An evaluation of multidrug-resistant Escherichia coli isolates in urinary tract infections from Aguascalientes, Mexico: cross-sectional study. Ann Clin Microbiol Antimicrob 17:34. https://doi.org/10.1186/s12941-018-0286-510.1186/s12941-018-0286-5 ↗
22. Bassetti M, Righi E, Carnelutti A et al (2018) Multidrug-resistant Klebsiella pneumoniae: challenges for treatment, prevention and infection control. Expert Rev Anti Infect Ther 16:749–761. https://doi.org/10.1080/14787210.2018.152224910.1080/14787210.2018.1522249 ↗
23. Grady R, Hayes F (2003) Axe-Txe, a broad-spectrum proteic toxin-antitoxin system specified by a multidrug-resistant, clinical isolate of Enterococcus faecium. Mol Microbiol 47:1419–1432. https://doi.org/10.1046/j.1365-2958.2003.03387.x10.1046/j.1365-2958.2003.03387.x ↗
24. Hiramatsu K, Katayama Y, Matsuo M et al (2014) Multi-drug-resistant Staphylococcus aureus and future chemotherapy. J Infect Chemother 20:593–601. https://doi.org/10.1016/j.jiac.2014.08.00110.1016/j.jiac.2014.08.001 ↗
25. Alamu EO, Maziya-Dixon B, Menkir A, et al (2021) Bioactive composition and free radical scavenging activity of fresh orange maize hybrids: impacts of genotype, maturity stages, and processing methods. Front Nutr 8:640563–640568.10.1076/1388-0209(200007)3831-SFT204 ↗
26. Rajani M, Shrivastava N, Ravishankara MN (2000) A rapid method for isolation of andrographolide from Andrographis Paniculata Nees (Kalmegh). Pharm Biol 38:204–209. https://doi.org/10.1076/1388-0209(200007)3831-SFT20410.1076/1388-0209(200007)3831-SFT204 ↗
27. Hailing Y, Xiufang L, Lili W et al (2020) Doxorubicin-loaded fluorescent carbon dots with PEI passivation as a drug delivery system for cancer therapy. Nanoscale 12:17222–17237. https://doi.org/10.1039/D0NR01236J10.1039/D0NR01236J ↗
28. Kong T, Hao L, Wei Y et al (2018) Doxorubicin conjugated carbon dots as a drug delivery system for human breast cancer therapy. Cell Prolif 51:e12488–e12494. https://doi.org/10.1111/cpr.1248810.1111/cpr.12488 ↗
29. Yuan Y, Guo B, Hao L et al (2017) Doxorubicin-loaded environmentally friendly carbon dots as a novel drug delivery system for nucleus targeted cancer therapy. Colloids Surf, B 159:349–359. https://doi.org/10.1016/j.colsurfb.2017.07.03010.1016/j.colsurfb.2017.07.030 ↗
30. Hu S, Yang W, Li N et al (2018) Carbon-dot-based heterojunction for engineering band-edge position and photocatalytic performance. Small 14:1803447–1803453. https://doi.org/10.1002/smll.20180344710.1002/smll.201803447 ↗
31. Zhang M, Ju H, Zhang L et al (2015) Engineering iodine-doped carbon dots as dual-modal probes for fluorescence and X-ray CT imaging. Int J Nanomed 10:6943–6953. https://doi.org/10.2147/IJN.S8277810.2147/IJN.S82778 ↗
32. Nigam P, Waghmode S, Louis M et al (2014) Graphene quantum dots conjugated albumin nanoparticles for targeted drug delivery and imaging of pancreatic cancer. J Mater Chem B 2:3190–3195. https://doi.org/10.1039/C4TB00015C10.1039/C4TB00015C ↗
33. Shamsipour M, Mansouri AM, Moradipour P (2019) Temozolomide conjugated carbon quantum dots embedded in core/shell nanofibers prepared by coaxial electrospinning as an implantable delivery system for cell imaging and sustained drug release. AAPS PharmSciTech 20:259–272. https://doi.org/10.1208/s12249-019-1466-010.1208/s12249-019-1466-0 ↗
34. Singh B, Singh S, Gautam A et al (2022) Preparation and characterization of PLA microspheres as drug delivery system for controlled release of Cetirizine with carbon dots as drug carrier. Polym Bull. https://doi.org/10.1007/s00289-022-04331-x10.1007/s00289-022-04331-x ↗
35. Saneja A, Kumar R, Singh A et al (2017) Development and evaluation of long-circulating nanoparticles loaded with betulinic acid for improved anti-tumor efficacy. Int J Pharm 531:153–166. https://doi.org/10.1016/j.ijpharm.2017.08.07610.1016/j.ijpharm.2017.08.076 ↗
36. Saraswat V, Kumari R, Yadav M (2022) Novel carbon dots as efficient green corrosion inhibitor for mild steel in HCl solution: electrochemical, gravimetric and XPS studies. J Phys Chem Solids 160:110341–110349. https://doi.org/10.1016/j.jpcs.2021.11034110.1016/j.jpcs.2021.110341 ↗
37. Liu J, Kong T, Xiong H-M (2022) Mulberry-leaves-derived red-emissive carbon dots for feeding silkworms to produce brightly fluorescent silk. Adv Mater 34:e2200152–e2200157. https://doi.org/10.1002/adma.20220015210.1002/adma.202200152 ↗
38. Du J, Xu N, Fan J et al (2019) Carbon dots for in vivo bioimaging and theranostics. Small 15:e1805087–e1805099. https://doi.org/10.1002/smll.20180508710.1002/smll.201805087 ↗
39. Kailasa SK, Ha S, Baek SH et al (2019) Tuning of carbon dots emission color for sensing of Fe3+ ion and bioimaging applications. Mater Sci Eng C Mater Biol Appl 98:834–842. https://doi.org/10.1016/j.msec.2019.01.00210.1016/j.msec.2019.01.002 ↗
40. Tian X, Chen L, Li Y et al (2017) Design and synthesis of a molecule with aggregation-induced emission effects and its application in the detection of arsenite in groundwater. J Mater Chem 5:3669–3672. https://doi.org/10.1039/C7TC00363C10.1039/C7TC00363C ↗
41. Highly Selective Turn-On Fluorogenic Chemosensor for Robust Quantification of Zn(II) Based on Aggregation Induced Emission Enhancement Feature | ACS Sensors. https://pubs.acs.org/doi/full/https://doi.org/10.1021/acssensors.6b00289?casa_token=5KQns-7-RRAAAAAA%3ApLQzrjEN5CMGcMs7mrspJghOxeum1qd19ak2VYejR_ntIr9QHGHHZ9pPDeTLZxpmsBxQtxDfHvxgV2M-dQ. Accessed 27 Mar 202310.1021/acssensors.6b00289?casa_token=5KQns-7-RRAAAAAA%3ApLQzrjEN5CMGcMs7mrspJghOxeum1qd19ak2VYejR_ntIr9QHGHHZ9pPDeTLZxpmsBxQtxDfHvxgV2M-dQ ↗
42. Chen J, Law CCW, Lam JWY et al (2003) Synthesis, light emission, nanoaggregation, and restricted intramolecular rotation of 1,1-Substituted 2,3,4,5-Tetraphenylsiloles. Chem Mater 15:1535–1546. https://doi.org/10.1021/cm021715z10.1021/cm021715z ↗
43. Kumar ASK, Jiang S-J (2017) Synthesis of magnetically separable and recyclable magnetic nanoparticles decorated with β-cyclodextrin functionalized graphene oxide an excellent adsorption of As(V)/(III). J Mol Liq 237:387–401. https://doi.org/10.1016/j.molliq.2017.04.09310.1016/j.molliq.2017.04.093 ↗
44. Gurung S, Neha, Arun N, et al (2023) Dual metal ion (Fe3+ and As3+) sensing and cell bioimaging using fluorescent carbon quantum dots synthesised from Cynodon dactylon. Chemosphere 339:139638–139646. https://doi.org/10.1016/j.chemosphere.2023.13963810.1016/j.chemosphere.2023.139638 ↗
45. Bayazeed Alam M, Hassan N, Sahoo K et al (2022) Deciphering interaction between chlorophyll functionalized carbon quantum dots with arsenic and mercury toxic metals in water as highly sensitive dual-probe sensor. J Photochem Photobiol A: Chem 431:114059–114071. https://doi.org/10.1016/j.jphotochem.2022.11405910.1016/j.jphotochem.2022.114059 ↗
46. Zhao X, Liao S, Wang L et al (2019) Facile green and one-pot synthesis of purple perilla derived carbon quantum dot as a fluorescent sensor for silver ion. Talanta 201:1–8. https://doi.org/10.1016/j.talanta.2019.03.09510.1016/j.talanta.2019.03.095 ↗
47. Qi H, Teng M, Liu M et al (2019) Biomass-derived nitrogen-doped carbon quantum dots: highly selective fluorescent probe for detecting Fe3+ ions and tetracyclines. J Colloid Interface Sci 539:332–341. https://doi.org/10.1016/j.jcis.2018.12.04710.1016/j.jcis.2018.12.047 ↗
48. Khan ZMSH, Rahman RS, Shumaila et al (2019) Hydrothermal treatment of red lentils for the synthesis of fluorescent carbon quantum dots and its application for sensing Fe3+. Optic Mater 91:386–395. https://doi.org/10.1016/j.optmat.2019.03.05410.1016/j.optmat.2019.03.054 ↗
49. Wang J, Sheng Li R, Zhi Zhang H et al (2017) Highly fluorescent carbon dots as selective and visual probes for sensing copper ions in living cells via an electron transfer process. Biosens Bioelectron 97:157–163. https://doi.org/10.1016/j.bios.2017.05.03510.1016/j.bios.2017.05.035 ↗
50. Liu R, Gao M, Zhang J et al (2015) An ionic liquid promoted microwave-hydrothermal route towards highly photoluminescent carbon dots for sensitive and selective detection of iron(III). RSC Adv 5:24205–24209. https://doi.org/10.1039/C5RA00089K10.1039/C5RA00089K ↗
51. Zhu S, Meng Q, Wang L et al (2013) Highly photoluminescent carbon dots for multicolor patterning, sensors, and bioimaging. Angew Chem Int Ed 52:3953–3957. https://doi.org/10.1002/anie.20130051910.1002/anie.201300519 ↗
52. Cancer statistics, 2023 - Siegel - 2023 - CA: A Cancer Journal for Clinicians - Wiley Online Library. https://acsjournals.onlinelibrary.wiley.com/doi/https://doi.org/10.3322/caac.21763. Accessed 25 Mar 202310.3322/caac.21763 ↗
53. Liao H-C, Chou Y-J, Lin C-C et al (2019) Andrographolide and its potent derivative exhibit anticancer effects against imatinib-resistant chronic myeloid leukemia cells by downregulating the Bcr-Abl oncoprotein. Biochem Pharmacol 163:308–320. https://doi.org/10.1016/j.bcp.2019.02.02810.1016/j.bcp.2019.02.028 ↗
54. Yang T, Yao S, Zhang X, Guo Y (2016) Andrographolide inhibits growth of human T-cell acute lymphoblastic leukemia Jurkat cells by downregulation of PI3K/AKT and upregulation of p38 MAPK pathways. Drug Des Devel Ther 10:1389–1397. https://doi.org/10.2147/DDDT.S9498310.2147/DDDT.S94983 ↗
55. Zhao D, Li X, Xu M et al (2023) Preparations of antibacterial yellow-green-fluorescent carbon dots and carbon dots-lysozyme complex and their applications in bacterial imaging and bacteria/biofilm inhibition/clearance. Int J Biol Macromol 231:123303–123311. https://doi.org/10.1016/j.ijbiomac.2023.12330310.1016/j.ijbiomac.2023.123303 ↗
56. Zhao D, Xu M, Dai K et al (2023) The preparation of chiral carbon dots and the study on their antibacterial abilities. Mater Chem Phys 295:127144. https://doi.org/10.1016/j.matchemphys.2022.12714410.1016/j.matchemphys.2022.127144 ↗
57. Hajipour MJ, Fromm KM, Akbar Ashkarran A et al (2012) Antibacterial properties of nanoparticles. Trends Biotechnol 30:499–511. https://doi.org/10.1016/j.tibtech.2012.06.00410.1016/j.tibtech.2012.06.004 ↗
58. Naik GG, Alam MB, Pandey V, Mohapatra D et al (2020) Multi-functional carbon dots from an ayurvedic medicinal plant for cancer cell bioimaging applications. J Fluoresc 30:407–41810.1007/s10895-020-02515-0 ↗