2022
DOI: 10.3390/nano12172954
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Box–Behnken Design: Optimization of Proanthocyanidin-Loaded Transferosomes as an Effective Therapeutic Approach for Osteoarthritis

Abstract: Transferosomes are one of the vesicular carriers that have received extensive research and attention recently because of their capacity to get beyond the barriers posed by the stratum corneum to penetration. The intent of the current study is to optimize and evaluate proanthocyanidin (PAC) containing transferosomal transdermal gels. PAC-containing transferosomes were prepared using the film hydration method and then loaded into a 4% methylcellulose gel. A 23 Box–Behnken design was used to optimize the PAC-load… Show more

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Cited by 17 publications
(8 citation statements)
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“…ZnO‐NPs were dispersed in a 0.9 % sodium chloride solution. The sample with a concentration of 0.01 % was transferred to a zeta dip cell for analysis [25] …”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…ZnO‐NPs were dispersed in a 0.9 % sodium chloride solution. The sample with a concentration of 0.01 % was transferred to a zeta dip cell for analysis [25] …”
Section: Methodsmentioning
confidence: 99%
“…The sample was laid out on a carbon‐coated grid to create a thin film and dried under the mercury lamp for 5 min. The SEM image of the ZnO‐NPs was recorded [25] …”
Section: Methodsmentioning
confidence: 99%
“…RSM is a combination of mathematical and statistical methods to seek the best conditions in a multifactor system, to model and analyze response problems influenced by multiple variables, to shorten the optimization time, and to improve the credibility of the application; the method has a low number of experiments, short cycle time, and high accuracy (Tamilarasan et al, 2022). For traditional mathematical and statistical methods, OFAT experiments can only consider the influence of a single factor and cannot determine whether there is an interaction between the factors.…”
Section: Discussionmentioning
confidence: 99%
“…Subsequentially, mixture was homogenised then transferred to a round bottom flask and placed on a rotary evaporator (Heidolph Laborota 4000 Series, Heizbad, Germany) at 100 rpm under reduced pressure at 60 °C, where a dry thin coating formed on the inner flask wall. Film was hydrated further with phosphate buffer pH 7.4 at 50 °C (5–10 °C above the amphiphiles phase transition temperature) [ 57 , 58 ]. After being kept at room temperature for 4 h, it was sonicated for specified time, as per design, to shatter the multilamellar phytosomes [ 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…Samples were removed periodically and physical appearance, particle size, drug content, and % EE were analysed. [ 57 , 58 ].…”
Section: Methodsmentioning
confidence: 99%