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. 2021 Jul 10;11:104. doi: 10.1186/s13568-021-01261-1

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Illustrating the average particle size distribution histogram and zeta potential of ZnO nanoparticle, the reducing/capping agent and various drugs used in the study where A showing particle size (a) and zeta potential graph (b) of quercetin loaded beta-cyclodextrin capped ZnO NPs (QT-ZnO-BCD NPs), B showing particle size distribution histogram (a) and zeta potential graph (b) of naringin loaded beta-cyclodextrin capped ZnO NPs (NAR-ZnO-BCD NPs), C display average particle size distribution histogram (a) and zeta potential graph (b) of ceftriaxone loaded beta-cyclodextrin capped ZnO NPs (CFT-ZnO-BCD NPs), D display particle size distribution histogram (a) and zeta potential graph (b) of ampicillin loaded beta-cyclodextrin capped ZnO nanoparticles (AMP-ZnO-BCD NPs) and E showing particle size distribution histogram (a) and zeta potential graph (b) of amphotericin B loaded beta-cyclodextrin capped ZnO nanoparticles (AMB-ZnO-BCD NPs)