2016
DOI: 10.1016/j.pdpdt.2016.06.010
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Immobilization of chlorophyll by using layer-by-layer technique for controlled release systems and photodynamic inactivation

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Cited by 7 publications
(3 citation statements)
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“…Thus, in order to preserve the monomeric state of the PS, to protect it from aqueous environment, and to increase the efficacy of photodynamic treatment, several transporters and delivery systems, such as liposomes, have also been developed in the last few years. Liposomes became known due to their high loading capacity, biodegradability, biocompatibility, and size [ 153 ]. In fact, these liposomal vesicles with one or more concentric phospholipid bilayer(s) have two main advantages in PDI ( Figure 31 ).…”
Section: Liposomesmentioning
confidence: 99%
“…Thus, in order to preserve the monomeric state of the PS, to protect it from aqueous environment, and to increase the efficacy of photodynamic treatment, several transporters and delivery systems, such as liposomes, have also been developed in the last few years. Liposomes became known due to their high loading capacity, biodegradability, biocompatibility, and size [ 153 ]. In fact, these liposomal vesicles with one or more concentric phospholipid bilayer(s) have two main advantages in PDI ( Figure 31 ).…”
Section: Liposomesmentioning
confidence: 99%
“…The relation between α and df of a surface can be obtained by: df = D-α, where D is the dimension of the space observed [39]. The interface-forming process that determines the surface morphology can be investigated using fractal concepts and dynamic-scale laws [39,40], which can be done by analyzing the log-log dependency of W as a function of the scan window length (L). In the linear region, wherein the laws of scale are satisfied, the value of the angular coefficient gives α [39].…”
Section: Discussionmentioning
confidence: 99%
“…The low concentration of PS ensures that it is possible to observe colony growth after PDI, as indicated by Freire et al [11] who observed that higher concentrations of eosin lead to cell death. To prepare fungal dispersions, one isolated colony was seeded from the original culture onto a Sabouraud agar plate and incubated at 37 °C for 24 h. Subsequently, 9.0 mg of the resulting culture was dispersed in 10 mL of physiological solution or in 10 mL of eosin solution (for inactivation experiments) [12][13][14].…”
Section: Methodsmentioning
confidence: 99%