1.A photothermal/chemotherapy injectable paclitaxel gel with irradiation stability.
Yaowen OUYANG ; Kui ZHANG ; Liangqin ZHOU ; Yuanwei CHEN ; Xianglin LUO
Journal of Biomedical Engineering 2021;38(5):979-985
		                        		
		                        			
		                        			The aim of this study is to construct an injectable gel with stable phototherapy and chemotherapy. Res-PTX@IR780 gel with phototherapy and chemotherapy property was prepared by introduction of photosensitizer IR780 and antioxidant resveratrol (Res) into the polyethylene glycol (PEG) solution of paclitaxel (PTX). The results showed that PTX, PTX@IR780 and Res-PTX@IR780 could form gels and the gels were injectable. ATR-FTIR results indicated not only components of the gels but also the formation of hydrogen bonding during the gelation. The results of UV showed instability of IR780 solution and stability improvement of Res-IR780 solution under infrared radiation (IR) irradiation. Photothermal tests showed that Res-PTX@IR780 displayed better photothermal conversion and photothermal stability under multiple irradiations than PTX@IR780. The results of
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Cell Line, Tumor
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Hyperthermia, Induced
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mice, Inbred BALB C
		                        			;
		                        		
		                        			Nanoparticles
		                        			;
		                        		
		                        			Paclitaxel
		                        			;
		                        		
		                        			Phototherapy
		                        			
		                        		
		                        	
2.Preparation of compound liquorice microemulsion gel and its pharmacodynamics evaluation.
Jing-Yan WANG ; M A SHU-WEI ; Xin-Yu ZHAO ; Jia-Jia CHEN ; Yu-Juan LIU ; Li-Li DENG ; Zi-You GUO ; W U QING
China Journal of Chinese Materia Medica 2020;45(21):5193-5199
		                        		
		                        			
		                        			Based on the previous study of compound liquorice microemulsion, this paper aims to prepare the compound liquorice microemulsion gel and investigate its pharmacodynamics of chronic eczema. The type, dosage and adding method of gel matrix, and formula dosage of humectant were optimized by single factor method to obtain the formula and preparation technique of the gel. With glycyrrhizic acid, glycyrrhetin and oxymatrine used as evaluation indexes, the Franz diffusion cell method was adopted to monitor the in vitro release profile of the gel. Eczema model of delayed-type hypersensitivity in mice was chosen to detect the ear swelling rate, degree of inflammatory cell infiltration of ear pieces, and pathological changes of ear pieces, so as to investigate the therapeutic effect of the microemulsion gel. The preparation process of the compound liquorice microemulsion gel was stable. The release of glycyrrhizin and oxymatrine was most consistent with the Hixcon-Crowell kinetic model, while the release of glycyrrhizic acid was most consistent with the Ritger-Peppas kinetic model. The pharmacodynamics studies proved that compound liquorice microemulsion gel could significantly reduce the ear swelling rate in mice, with good anti-inflammatory effect as well as the ability to resist the pathological changes of chronic eczema and inhibit the infiltration of dermal inflammatory cells. Therefore, the preparation process of compound liquorice microemulsion gel is feasible, with stable drug release and a significant therapeutic effect on chronic eczema.
		                        		
		                        		
		                        		
		                        			Administration, Cutaneous
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Drug Liberation
		                        			;
		                        		
		                        			Emulsions
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Glycyrrhiza
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Skin Absorption
		                        			
		                        		
		                        	
3.Rheology and in vitro release properties of thermosensitive in situ gel of Yihuang Decoction and its common gel for vaginal use.
Xiu-Qing WANG ; Yu-Ling LIU ; Long-Fei LIN ; Ji-Zheng SONG ; Yu-Ting LUO ; Hui LI
China Journal of Chinese Materia Medica 2020;45(3):539-547
		                        		
		                        			
		                        			To evaluate the traits and rheological properties of thermosensitive in situ gel of Yihuang Decoction and its common gel for vaginal use, and predict the release behavior of Yihuang Decoction in situ gel in vitro. Poloxamer was used as thermosensitive material to prepare Yihuang Decoction vaginal in situ gel, and Yihuang Decoction common gel was prepared with carbopol. Then the differences of the two gels before and after diluting with vaginal fluid were compared. The rheological parameters of Yihuang Decoction in situ gel and its common gel were determined with Anton Paar MCR102 rheometer. In addition, berberine hydrochloride was selected as an index component to evaluate the in vitro release properties of Yihuang Decoction vaginal thermosensitive in situ gel. Yihuang Decoction vaginal thermosensitive in situ gel was Newtonian fluid under low-temperature conditions, which was yellow and transparent. After reaching the gelling temperature of 24.5 ℃, it became semi-solid, pseudoplastic fluid. The gelling temperature was predicted to be 37 ℃, and the phase transition time was 30 s after diluting with simulated vaginal fluid. However, the rheological properties of Yihuang Decoction common gel had no significant changes with temperature. Compared with in situ gel, the color of common gel was darker and more translucent. Besides, its mobility was stronger after diluting with simulated vaginal fluid. The in vitro release study showed that the kinetic behavior of berberine hydrochloride in Yihuang Decoction vaginal thermosensitive in situ gel was matched with the Higuchi equation. Through simulation of vaginal administration, physical properties and dynamic rheological parameters were used to intuitively and scientifically evaluate the two gels. Compared with the common gel, the thermosensitive in situ gel could quickly attached to the vaginal mucosa and release drug, and thus was more suitable for developing vaginal administration of Yihuang Decoction, which also provides references for studying new vaginal preparation of Yihuang Decoction.
		                        		
		                        		
		                        		
		                        			Administration, Intravaginal
		                        			;
		                        		
		                        			Drugs, Chinese Herbal/chemistry*
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		                        			Female
		                        			;
		                        		
		                        			Gels/chemistry*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Poloxamer
		                        			;
		                        		
		                        			Rheology
		                        			;
		                        		
		                        			Temperature
		                        			;
		                        		
		                        			Viscosity
		                        			
		                        		
		                        	
4.Pharmacokinetics of skin and blood of Tripterygium wilfordii and Paeonia lactiflora micro-emulsion gel based on micro-dialysis technology.
Qing DU ; Jing LUO ; Yong-Mei GUAN ; Fang XIAO ; Zhen-Zhong ZANG ; Chen JIN ; Li-Hua CHEN
China Journal of Chinese Materia Medica 2019;44(16):3569-3575
		                        		
		                        			
		                        			To further investigate the metabolism of Tripterygium wilfordii and Paeonia lactiflora micro-emulsion gel in vivo,an LCMS/MS method was established for the determination of triptolide and paeoniflorin in T. wilfordii and P. lactiflora micro-emulsion gel.The extracorporeal recovery rate of blood probe was measured by concentration difference methods( incremental method and decremental method). Meanwhile,the skin and blood micro-dialysis methods of tripterine and paeoniflorin were established,and the pharmacokinetics of T. wilfordii microemulsion gel in skin and blood was studied by micro-dialysis combined with LC-MS/MS quantitative analysis. The results showed that the established method for the determination of triptolide and paeoniflorin in T. wilfordii microemulsion gel was well linear within the required range,and the specificity,recovery rate and degree of precision of the chromatography all conformed to the research requirements of micro-dialysis samples. The stability of freeze-thawing and the residual effect all conformed to the criteria of biological sample methodology. The probe recovery rates measured by incremental method and decremental method were almost consistent with the extracorporeal recovery rate test. The recovery rates of paeoniflorin in skin and blood micro-dialysis were( 30. 60±1. 09) % and( 28. 01± 1. 75) %,respectively. And the recovery rates of skin and blood micro-dialysis were( 26. 79 ± 2. 78) % and( 25. 39±1. 86) %,respectively. The intraday recovery rate of probes was stable within 11 h. The results of pharmacokinetic study showed that the Cmaxvalues of triptolide in skin and blood were( 148. 03±41. 51) and( 76. 77±15. 27) μg·L-1,respectively. And the Tmaxvalues were( 2. 33±0. 29) and( 3. 00± 0) h,respectively. The AUC0-11 hvalues were( 2 814. 05± 1 070. 37) and( 1 580. 63±208. 27) μg·h·L-1,respectively. The MRT0-11 hvalues were( 4. 20± 0. 33) and( 4. 54± 0. 34) h,respectively. The T1/2 values were( 4. 61±4. 11) and( 1. 07± 0. 13) h,respectively. The Cmaxvalues of paeoniflorin in skin and blood were( 991. 88 ± 152. 22) and( 407. 02±120. 06) μg·L-1,respectively. The Tmaxvalues were( 2. 00±0) h and( 2. 83±0. 29) h,respectively. The AUC0-11 hvalues were( 18 430. 27±3 289. 35) and( 6 338. 59 ± 1 659. 32) μg·h·L-1,respectively. The MRT0-11 hvalues were( 4. 29 ± 0. 16) and( 4. 00±0. 05) h,respectively. The T1/2 values were( 2. 16±0. 43) and( 1. 78±0. 48) h,respectively. The results suggested that micro-emulsion gel played a role in forming skin reservoir through percutaneous penetration. It not only could improve drug transdermal efficiency,but also control the sustained release of drug and form a long-term effect.
		                        		
		                        		
		                        		
		                        			Blood
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Chromatography, Liquid
		                        			;
		                        		
		                        			Drugs, Chinese Herbal
		                        			;
		                        		
		                        			pharmacokinetics
		                        			;
		                        		
		                        			Emulsions
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Paeonia
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Skin
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Tandem Mass Spectrometry
		                        			;
		                        		
		                        			Tripterygium
		                        			;
		                        		
		                        			chemistry
		                        			
		                        		
		                        	
5.Preventive Effects of Fluoride Gel Application on Dental Caries in the Permanent Tooth: A Systematic Review of Randomized Controlled Trials
Journal of Dental Hygiene Science 2019;19(1):9-22
		                        		
		                        			
		                        			BACKGROUND: The purpose of this systematic review was to investigate the effects of topical fluoride gel application on dental caries prevention in the permanent teeth of children and adolescents. METHODS: We searched the EMBASE, PubMed, and Cochrane Library databases for randomized controlled trials (RCTs) assessing the effects of self-applied or professionally applied topical fluoride gels in patients <18 years of age; the search was completed on April 1, 2018. All included trials involved an experimental group (fluoride gel application) and a control group (placebo or no treatment). The outcome measures were the D(M)FS and D(M)FT indices, which were compared between the two groups. Review Manager software was used for quantitative synthesis of the final selected articles, and a forest plot was generated via a meta-analysis conducted using a random effects model. RESULTS: The results showed that the D(M)FS and D(M)FT indices were lower in the fluoride application group than in the control group, thus indicating that fluoride gel application was effective in dental caries prevention. We also performed a subgroup analysis to determine whether the effects of fluoride application differed if patients received oral prophylaxis (self or professional) before fluoride gel application. Therefore, the two groups showed slightly larger differences when studies without oral prophylaxis before fluoride gel application were considered; however, the difference was not statistically significant. CONCLUSION: These findings should be utilized to raise awareness about the caries-prevention effects of topical fluoride application among patients and guardians. Further RCTs should evaluate the effects of fluoride application with or without preceding oral prophylaxis, and appropriate fluoride application guidelines should be developed to maximize the effects of fluoride application in clinical practice.
		                        		
		                        		
		                        		
		                        			Adolescent
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Dental Caries
		                        			;
		                        		
		                        			Fluorides
		                        			;
		                        		
		                        			Forests
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Outcome Assessment (Health Care)
		                        			;
		                        		
		                        			Tooth
		                        			
		                        		
		                        	
6.Research progress on functional soft candy of traditional Chinese medicine.
Yan-Hong WANG ; Ning LUAN ; Jian FAN ; Hong-Jing LI ; Kai SHENG ; Da-Zhong CHEN
China Journal of Chinese Materia Medica 2019;44(24):5345-5351
		                        		
		                        			
		                        			Functional soft candy of traditional Chinese medicine( TCM) can be used to supplement vitamins,enhance immunity,assist in lowering blood sugar,assist in lowering blood lipid,assist in lowering blood pressure,relax the bowel,reduce weight and fight againstoxidation.It has attracted much attention due to its effective improvement in the bad taste and incompatibility of traditional medicines.TCM functional soft candy and health food made by gel,sweetener and Chinese herbal medicines( which can be used both as food and medicine) approved by the State Food and Drug Administration were selected as the research objects in this paper.We combed and analyzed the research situation of health food dosage forms and effects,the functional factors of TCM functional soft candy,gelatin,sweetener,production process,and quality evaluation,etc.,and then,we discussed their existing problems and development prospects.After reviewing the relevant literature on TCM functional soft candy and health food researches published in recent years,we analyzed and summarized their dosage forms,health effects,gels,sweeteners,production process,quality evaluation and safety.The following problems in the research of TCM functional soft candy were pointed out: for examples,differences in the sensory evaluation of soft candy;whether the combination of several similar gels and sweeteners had an effect on human health; the lack of laws and regulations in health foods and the lack of uniform standards for quality evaluation.In summary,TCM functional soft candy is a new type of health food,which changes the dosage form of health food based on capsules and tablets.This move conforms to the physiological and psychological needs of consumers.Therefore,it is in line with the requirement of " Health China 2030" Planning Outline.
		                        		
		                        		
		                        		
		                        			Candy
		                        			;
		                        		
		                        			China
		                        			;
		                        		
		                        			Dosage Forms
		                        			;
		                        		
		                        			Drugs, Chinese Herbal/administration & dosage*
		                        			;
		                        		
		                        			Food
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Medicine, Chinese Traditional
		                        			;
		                        		
		                        			Reference Standards
		                        			
		                        		
		                        	
7.Role of Hydrogen Sulfide in the Survival of Fibroblasts and Fibroblast-mediated Contraction of Collagen Gel
Journal of the Korean Ophthalmological Society 2019;60(10):975-981
		                        		
		                        			
		                        			PURPOSE: To investigate the role of hydrogen sulfide in the survival and collagen gel contraction of cultured human Tenon's capsule fibroblasts (HTCFs). METHODS: Primarily cultured HTCFs were exposed to 0, 100, 200, or 300 µM hydrogen sulfide (sodium hydrogen sulfide, NaHS) for 2 days. Cellular survival was assessed by MTT (3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyltetrazolium bromide) assay. Degree of apoptosis was assessed with flow cytometry using annexin-V/propidium iodide double staining. To evaluate the effect of NaHS on cellular transdifferentiation, HTCFs were stimulated with 5 ng/mL TGF-β1 and the level of expression of α-smooth muscle actin (SMA) mRNA was assessed using reverse-transcription polymerase chain reaction. The cells were embedded in collagen gel, and the amount of gel contraction was measured. RESULTS: NaHS at 300 µM reduced HTCF survival (p = 0.013); NaHS at both 200 and 300 µM increased apoptosis in a dose-dependent manner (p = 0.013 and p = 0.016). TGF-β1 increased the expression of α-SMA mRNA (p = 0.041); co-treatment with 100 µM NaHS decreased TGF-β1-induced α-SMA mRNA expression (p = 0.039) and inhibited collagen gel contraction. CONCLUSIONS: NaHS at high concentration reduced cellular survival and increased HTCF apoptosis. NaHS decreased TGF-β 1-induced increases in α-SMA mRNA expression and collagen gel contraction. Thus, hydrogen sulfide may suppress scar formation by inhibiting HTCF transdifferentiation and contraction of collagen gels.
		                        		
		                        		
		                        		
		                        			Actins
		                        			;
		                        		
		                        			Apoptosis
		                        			;
		                        		
		                        			Cicatrix
		                        			;
		                        		
		                        			Collagen
		                        			;
		                        		
		                        			Fibroblasts
		                        			;
		                        		
		                        			Flow Cytometry
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hydrogen Sulfide
		                        			;
		                        		
		                        			Hydrogen
		                        			;
		                        		
		                        			Polymerase Chain Reaction
		                        			;
		                        		
		                        			RNA, Messenger
		                        			;
		                        		
		                        			Tenon Capsule
		                        			
		                        		
		                        	
8.Tooth whitening effects of manicure-type hydrogen peroxide tooth whitening gel
Yong Gwan KIM ; Ji Hyeon PARK ; Ja Won CHO
Journal of Korean Academy of Oral Health 2019;43(4):191-195
		                        		
		                        			
		                        			OBJECTIVES: To examine the tooth whitening effects of a 3% hydrogen peroxide gel.METHODS: Twenty participants were given experimental tooth whitening gels containing 3% hydrogen peroxide, and another 20 participants, who served as the control group, were given tooth whitening gels that contained no hydrogen peroxide. Both groups used their respective whitening agents for 1 week, and tooth lightness was examined at baseline and 4 and 7 days after the experiment.RESULTS: Compared with the control group, in the experimental group, lightness values, determined using VITA classical A1-D4® and VITA SYSTEM 3D-MASTER®, were significantly increased after using the 3% hydrogen peroxide whitening agent (P < 0.01) both 5 and 7 days post-application (P < 0.05).CONCLUSIONS: The study findings confirmed that an improved tooth whitening effect could be expected with the use of a new type of whitening gel containing 3% hydrogen peroxide.
		                        		
		                        		
		                        		
		                        			Bleaching Agents
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Hydrogen Peroxide
		                        			;
		                        		
		                        			Hydrogen
		                        			;
		                        		
		                        			Tooth Bleaching
		                        			;
		                        		
		                        			Tooth
		                        			;
		                        		
		                        			Toothpastes
		                        			
		                        		
		                        	
9.Evaluation of Microtensile Bond Strength of Sealant Depending on the Duration of Etching and the Use of Bonding Agent
Seoyoun SHIM ; Hojun SONG ; Sunmi YANG ; Jaehwan KIM ; Seonmi KIM ; Namki CHOI
Journal of Korean Academy of Pediatric Dentistry 2018;45(3):299-305
		                        		
		                        			
		                        			The aim of this study was to evaluate the effect of etching time and bonding agents on bond strength of sealant applied to the occlusal surface of primary molars.Forty non-carious exfoliated human primary molars were included in the study. The teeth were randomly divided into 4 groups for measurement. For group I, no acid etching treatment was used. For group II, III, and IV, acid etching gels were applied on the occlusal surface for 15, 30, and 60 seconds, respectively. Each group was divided into 2 subgroups; one group was treated with bonding agents on the enamel while the other was not. Microtensile bond strength was evaluated using a universal testing machine.There were no statistically significant differences in bond strength with varying duration of etching among groups. The results revealed that the use of bonding agents prior to application of fissure sealant increased the bond strength(p < 0.05).It could be concluded that etching time greater than 15 seconds does not significantly enhance the bond strength, but the use of bonding agents as an intermediate layer between the primary molar and fissure sealant would be beneficial in increasing the bond strength.
		                        		
		                        		
		                        		
		                        			Dental Enamel
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Molar
		                        			;
		                        		
		                        			Pit and Fissure Sealants
		                        			;
		                        		
		                        			Tooth
		                        			
		                        		
		                        	
10.Efficacy and safety of newly developed cross-linked dextran gel injection for glans penis augmentation with a novel technique.
Dae Yul YANG ; Kyungtae KO ; Seong Ho LEE ; Du Geon MOON ; Jong Wook KIM ; Won Ki LEE
Asian Journal of Andrology 2018;20(1):80-84
		                        		
		                        			
		                        			There is no safe and effective standard method for glans penis augmentation. Furthermore, there has been scant research on glans penis augmentation due to a poor understanding of glans anatomy, technical difficulty, and a lack of suitable substances for augmentation. Cross-linked dextran gel is a newly developed filler for soft-tissue augmentation. We evaluated the efficacy and safety of using a novel technique to inject cross-linked dextran gel for glans penis augmentation during a 24-week follow-up study. This prospective, single-arm, multicenter study enrolled twenty healthy adult men who underwent glans penis augmentation between June and August 2013. Cross-linked dextran gel was injected into the glans penis using a simple and easy technique. The sizes of the glans penis and individual satisfaction were assessed. Any adverse event was also reported. A total of 18 individuals were analyzed; two of them were lost to follow-up. The mean procedure time and injected volume were about 30 min and 6.6 ± 0.9 ml, respectively. The mean surface areas of the glans at baseline and 24 weeks were 20.0 ± 3.5 cm2 and 33.6 ± 5.4 cm2 , respectively, representing a mean increase of 68.7% ± 14.0% (P < 0.001). Sixteen individuals (88.9%) were satisfied with the outcomes, and none were dissatisfied. There were no serious adverse events during the study. Cross-linked dextran gel injection for glans penis augmentation was easy and showed a significant augmentative effect on the glans penis, good durability, and was well tolerated without serious adverse events. Therefore, cross-linked dextran gel injection may be an effective, new technique for glans penis augmentation.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Cross-Linking Reagents
		                        			;
		                        		
		                        			Dextrans/therapeutic use*
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Gels
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Injections
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Patient Satisfaction
		                        			;
		                        		
		                        			Penis/anatomy & histology*
		                        			;
		                        		
		                        			Prospective Studies
		                        			;
		                        		
		                        			Treatment Outcome
		                        			;
		                        		
		                        			Young Adult
		                        			
		                        		
		                        	
            
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