2017
DOI: 10.1016/j.carbpol.2016.09.058
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Development of bacterial cellulose based slow-release active films by incorporation of Scrophularia striata Boiss. extract

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Cited by 77 publications
(31 citation statements)
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“…Three categories of nanocellulose materials have been described as drug carriers: planar hydrogels (fleeces, films, membranes, coatings) [410][411][412][413], CNFs [414,415] as well as CNCs [416][417][418][419], with the two latter preferentially formulated as nano-and microparticles, gels, or suspensions [9]. For the entrapment of drugs these materials were used in the wet native [37,420,421], dried (freeze-dried, critical point dried) [422] or semi-dried [413,423] form, as well as air-dried materials with a shape memory effect [29,424].…”
Section: Figure 16mentioning
confidence: 99%
See 1 more Smart Citation
“…Three categories of nanocellulose materials have been described as drug carriers: planar hydrogels (fleeces, films, membranes, coatings) [410][411][412][413], CNFs [414,415] as well as CNCs [416][417][418][419], with the two latter preferentially formulated as nano-and microparticles, gels, or suspensions [9]. For the entrapment of drugs these materials were used in the wet native [37,420,421], dried (freeze-dried, critical point dried) [422] or semi-dried [413,423] form, as well as air-dried materials with a shape memory effect [29,424].…”
Section: Figure 16mentioning
confidence: 99%
“…Still challenging is the controlled release of highly lipophilic drugs due to their incompatibility with the hydrophilic character of the nanocelluloses [412,426,432]. Cetyl trimethylammonium bromide-coated CNCs bound significant quantities of the hydrophobic drugs docetaxel, paclitaxel, and etoposide followed by about 20-26% release in the first hours and a longer release period of 2-4 days [432].…”
Section: Figure 16mentioning
confidence: 99%
“…For the development of dermal patches, the porosity of BC is easily exploited to load drugs with different features, ranging from antibacterial activity to anticancer properties . Additionally, BC can be further optimized by chemical modifications with other (bio)polymers or by producing BC‐based materials, to better control its cargo release, burst, or sustained release, and even responsive releases to pH, temperature, or electromagnetism . For the development of oral formulations, BC has been used in combination with other biopolymers for a controlled release of the drug within, e.g., for the oral delivery of insulin, and hydrophobic and hydrophilic drugs alike …”
Section: Applicationsmentioning
confidence: 99%
“…Natural antibacterial plant extracts like silymarin isolated from milk thistle have been used to make nanoparticles with zein, and immersing BC hydrogels in the silymarin-zein nanoparticle suspensions has been used to produce films which inhibited growth E. coli, S. aureus, and P. aeruginosa though more so for the air dried films as compared to the lyophilized films [140]. Other extracts, like scrophulariastriata boiss extract as well as mulberry leaf acid hydrolysate have been added to the growth media during production of BC films with the latter showing reduction in the growth of both E. coli and S. aureus which they attributed to antibacterial flavonoids of the mulberry leaf extract that were embedded in the bacterial cellulose for sustained release [141,142].…”
Section: Biomedical Application Area Key Features Refmentioning
confidence: 99%