BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Tian B, Liu Y, Liu J. Cyclodextrin as a magic switch in covalent and non-covalent anticancer drug release systems. Carbohydr Polym 2020;242:116401. [PMID: 32564836 DOI: 10.1016/j.carbpol.2020.116401] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Komiyama M. Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems. Beilstein J Nanotechnol 2023;14:218-32. [PMID: 36793325 DOI: 10.3762/bjnano.14.21] [Reference Citation Analysis]
2 Gao Y, Wang K, Zhang J, Duan X, Sun Q, Men K. Multifunctional nanoparticle for cancer therapy. MedComm (2020) 2023;4:e187. [PMID: 36654533 DOI: 10.1002/mco2.187] [Reference Citation Analysis]
3 Ghitman J, Voicu SI. Controlled drug delivery mediated by cyclodextrin-based supramolecular self-assembled carriers: From design to clinical performances. Carbohydrate Polymer Technologies and Applications 2022. [DOI: 10.1016/j.carpta.2022.100266] [Reference Citation Analysis]
4 Qin L, Cui Z, Wu Y, Wang H, Zhang X, Guan J, Mao S. Challenges and Strategies to Enhance the Systemic Absorption of Inhaled Peptides and Proteins. Pharm Res 2022. [DOI: 10.1007/s11095-022-03435-3] [Reference Citation Analysis]
5 Wang J, Qiu Y, Li L, Qi X, An B, Ma K, Kong J, Zhang X. A Multi − Site initiation reversible Addition − Fragmentation Chain − Transfer electrochemical cocaine sensing. Microchemical Journal 2022;181:107714. [DOI: 10.1016/j.microc.2022.107714] [Reference Citation Analysis]
6 Ienașcu IMC, Căta A, Ştefănuț MN, Popescu I, Rusu G, Sfîrloagă P, Ursu D, Moşoarcă C, Dabici A, Danciu C, Muntean D, Pop R. Novel Chloro-Substituted Salicylanilide Derivatives and Their β-Cyclodextrin Complexes: Synthesis, Characterization, and Antibacterial Activity. Biomedicines 2022;10:1740. [DOI: 10.3390/biomedicines10071740] [Reference Citation Analysis]
7 Meiczinger M, Varga B, Wolmarans L, Hajba L, Somogyi V. Stability improvement of laccase for micropollutant removal of pharmaceutical origins from municipal wastewater. Clean Techn Environ Policy. [DOI: 10.1007/s10098-022-02336-8] [Reference Citation Analysis]
8 Zhang X, Su J, Wang X, Wang X, Liu R, Fu X, Li Y, Xue J, Li X, Zhang R, Chu X. Preparation and Properties of Cyclodextrin Inclusion Complexes of Hyperoside. Molecules 2022;27:2761. [PMID: 35566111 DOI: 10.3390/molecules27092761] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
9 Tian B, Xu D, Li W, Wang J, Cheng J, Liu Y. Proteomic analysis of hexahydro-β-acids/hydroxypropyl-β-cyclodextrin inhibit Listeria monocytogenes. Appl Microbiol Biotechnol. [DOI: 10.1007/s00253-022-11764-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Zhang H, Liao X, Wu X, Shi C, Zhang Y, Yuan Y, Li W, Wang J, Liu Y. Iridium(III) complexes entrapped in liposomes trigger mitochondria-mediated apoptosis and GSDME-mediated pyroptosis. J Inorg Biochem 2022;228:111706. [PMID: 35033830 DOI: 10.1016/j.jinorgbio.2021.111706] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
11 Panagiotakis S, Mavroidi B, Athanasopoulos A, Charalambidis G, Coutsolelos AG, Paravatou-Petsotas M, Pelecanou M, Mavridis IM, Yannakopoulou K. Unsymmetrical, monocarboxyalkyl meso-arylporphyrins in the photokilling of breast cancer cells using permethyl-β-cyclodextrin as sequestrant and cell uptake modulator. Carbohydr Polym 2022;275:118666. [PMID: 34742406 DOI: 10.1016/j.carbpol.2021.118666] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Liu J, Tian B, Liu Y, Wan JB. Cyclodextrin-Containing Hydrogels: A Review of Preparation Method, Drug Delivery, and Degradation Behavior. Int J Mol Sci 2021;22:13516. [PMID: 34948312 DOI: 10.3390/ijms222413516] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Gandhi S, Shende P. Cyclodextrins-modified metallic nanoparticles for effective cancer therapy. J Control Release 2021;339:41-50. [PMID: 34560156 DOI: 10.1016/j.jconrel.2021.09.025] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
14 Rincón-López J, Almanza-Arjona YC, Riascos AP, Rojas-Aguirre Y. When Cyclodextrins Met Data Science: Unveiling Their Pharmaceutical Applications through Network Science and Text-Mining. Pharmaceutics 2021;13:1297. [PMID: 34452258 DOI: 10.3390/pharmaceutics13081297] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
15 Tian B, Liu Y, Liu J. Chitosan-based nanoscale and non-nanoscale delivery systems for anticancer drugs: A review. European Polymer Journal 2021;154:110533. [DOI: 10.1016/j.eurpolymj.2021.110533] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 6.5] [Reference Citation Analysis]
16 Jicsinszky L, Martina K, Cravotto G. Cyclodextrins in the antiviral therapy. J Drug Deliv Sci Technol 2021;64:102589. [PMID: 34035845 DOI: 10.1016/j.jddst.2021.102589] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
17 Petitjean M, García-Zubiri IX, Isasi JR. History of cyclodextrin-based polymers in food and pharmacy: a review. Environ Chem Lett 2021;:1-12. [PMID: 33907537 DOI: 10.1007/s10311-021-01244-5] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
18 Yang W, Yang L, Li F, Zhao Y, Liao X, Gao C, Yang J, Yang B. pH-sensitive β-cyclodextrin derivatives for the controlled release of Podophyllotoxin. Journal of Molecular Structure 2021;1228:129744. [DOI: 10.1016/j.molstruc.2020.129744] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
19 Chen XY, Yang HW, Chi SM, Yue LL, Ruan Q, Lei Z, Zhu HY, Zhao Y. Solubility and biological activity enhancement of docetaxel via formation of inclusion complexes with three alkylenediamine-modified β-cyclodextrins. RSC Adv 2021;11:6292-303. [PMID: 35423130 DOI: 10.1039/d0ra09720a] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
20 Nicolosi M, Bellia F, Giuffrida ML, Zimbone S, Oliveri V, Vecchio G. Synthesis and biological evaluation of novel β-cyclodextrin-fluvastatin conjugates. Results in Chemistry 2021;3:100230. [DOI: 10.1016/j.rechem.2021.100230] [Reference Citation Analysis]
21 Sandhya S, Devika V, Rajeev N, Sreelekshmi PJ, Chandran A, Goutami GB, Aiswarya Lakshmi S. Multiple stimuli responsive cyclodextrin based smart materials for drug delivery: a review. E3S Web Conf 2021;309:01014. [DOI: 10.1051/e3sconf/202130901014] [Reference Citation Analysis]
22 Wang Y, Han Y, Tan X, Dai Y, Xia F, Zhang X. Cyclodextrin capped gold nanoparticles (AuNP@CDs): from synthesis to applications. J Mater Chem B 2021;9:2584-93. [DOI: 10.1039/d0tb02857f] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
23 Reig-Vano B, Tylkowski B, Montané X, Giamberini M. Alginate-based hydrogels for cancer therapy and research. Int J Biol Macromol 2021;170:424-36. [PMID: 33383080 DOI: 10.1016/j.ijbiomac.2020.12.161] [Cited by in Crossref: 20] [Cited by in F6Publishing: 23] [Article Influence: 6.7] [Reference Citation Analysis]
24 Rivero-Barbarroja G, Benito JM, Ortiz Mellet C, García Fernández JM. Cyclodextrin-Based Functional Glyconanomaterials. Nanomaterials (Basel) 2020;10:E2517. [PMID: 33333914 DOI: 10.3390/nano10122517] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
25 Mohandoss S, Edison TNJI, Atchudan R, Palanisamy S, Prabhu NM, Napoleon AA, You S, Lee YR. Ultrasonic-assisted efficient synthesis of inclusion complexes of salsalate drug and β-cyclodextrin derivatives for potent biomedical applications. Journal of Molecular Liquids 2020;319:114358. [DOI: 10.1016/j.molliq.2020.114358] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
26 Liao R, Liu Y, Lv P, Wu D, Xu M, Zheng X. Cyclodextrin pendant polymer as an efficient drug carrier for scutellarin. Drug Deliv 2020;27:1741-9. [PMID: 33307844 DOI: 10.1080/10717544.2020.1856223] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
27 Sorroza-Martínez K, González-Méndez I, Vonlanthen M, Moineau-Chane Ching KI, Caminade AM, Illescas J, Rivera E. First Class of Phosphorus Dendritic Compounds Containing β-Cyclodextrin Units in the Periphery Prepared by CuAAC. Molecules 2020;25:E4034. [PMID: 32899600 DOI: 10.3390/molecules25184034] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
28 Tian B, Liu Y, Liu J. Smart stimuli-responsive drug delivery systems based on cyclodextrin: A review. Carbohydr Polym 2021;251:116871. [PMID: 33142550 DOI: 10.1016/j.carbpol.2020.116871] [Cited by in Crossref: 49] [Cited by in F6Publishing: 36] [Article Influence: 16.3] [Reference Citation Analysis]