Progress in Research of Photo-controlled Drug Delivery Systems

Abstract

The controlled drug delivery systems, due to their precise control of drug release in spatiotemporal level triggered by specific stimulating factors and advantages such as higher utilization ratio of drug, less side-effects to normal tissues and so forth, provide a new strategy for the precise treatment of many serious diseases, especially tumors. The materials that constitute the controlled drug delivery systems are called "smart materials" and they can respond to the stimuli of some internal (pH, redox, enzymes, etc.) or external (temperature, electrical/magnetic, ultrasonic and optical, etc.) environments. Before and after the response to the specific stimulus, the composition or conformational of smart materials will be changed, damaging the original balance of the delivery systems and releasing the drug from the delivery systems. Amongst them, the photo-controlled drug delivery systems, which display drug release controlled by light, demonstrated extensive potential applications, and received wide attention from researchers. In recent years, photo-controlled drug delivery systems based on different photo-responsive groups have been designed and developed for precise photo-controlled release of drugs. Herein, in this review, we introduced four photo-responsive groups including photocleavage groups, photoisomerization groups, photo-induced rearrangement groups and photocrosslinking groups, and their different photo-responsive mechanisms. Firstly, the photocleavage groups represented by O-nitrobenzyl are able to absorb the energy of the photons, inducing the cleavage of some specific covalent bonds. Secondly, azobenzenes, as a kind of photoisomerization groups, are able to convert reversibly between the apolar trans form and the polar cis form upon different light irradiation. Thirdly, 2-diazo-1,2-naphthoquinone as the representative of the photo-induced rearrangement groups will absorb specific photon energy, carrying out Wolff rearrangement reaction. Finally, coumarin is a promising category photocrosslinking groups that can undergo [2＋2] cycloaddition reactions under light irradiation. The research progress of photo-controlled drug delivery systems based on different photo-responsive mechanisms were mainly reviewed. Additionally, the existing problems and the future research perspectives of photo-controlled drug delivery systems were proposed.

Remote Light‐Responsive Nanocarriers for Controlled Drug Delivery: Advances and Perspectives

“…), and 3) photocross‐linking/‐decross‐linking (e.g., coumarin, cinnamoyl, etc.) . The polymer/nanoparticle design, light responsiveness, and drug release behavior of these three processes‐based drug delivery systems will be introduced in the following sections in detail and the involved nanocarrier systems were summarized in Table 1 .…”

Stimuli‐Responsive Lanthanide‐Based Smart Luminescent Materials for Optical Encoding and Bio‐applications

“…[55] Photo-controlled drug delivery systems, based on different photo-responsive groups such as photocleavage groups, photoisomerization groups, photo-induced rearrangement groups and photocrosslinking groups, have been designed and developed for precise photo-controlled release of drugs. [56] Selected photo-responsive groups and their response mechanism are shown as Figure 24. 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57…”

“…Photo‐controlled drug delivery systems, based on different photo‐responsive groups such as photocleavage groups, photoisomerization groups, photo‐induced rearrangement groups and photocrosslinking groups, have been designed and developed for precise photo‐controlled release of drugs . Selected photo‐responsive groups and their response mechanism are shown as Figure .…”

Electrochemical Derivatization of Acetaminophen for Indirect Determination of Eflornithine Using β‐CD Modified Glassy Carbon Electrode

“…Subsequently, these cations join to each other and finally leads to formation of electropolymerized β-CD [35]. Furthermore, the β-CD/GCE could provide a good electroanalytical performance due to its various advantages such as; reproducibility, good stability and high conductivity [36].…”