Anlin Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Anlin Wang has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Ligang Liu
Department of Pharmacy Practice and Administration, College of Pharmacy, Western University of Health Sciences, Pomona, CA 91766, USA
2 shared publications - Milap Chand Nahata
Institute of Therapeutic Innovations and Outcomes, College of Pharmacy, The Ohio State University, Columbus, USA
2 shared publications - Mohammad Azam
Department of Chemistry College of Science King Saud University Riyadh Saudi Arabia
2 shared publications Bin Gao
College of Chemistry, Chemical and Environmental Engineering, Weifang University, No. 5147 Dongfeng Street, Weifang, 261061, P. R. China
1 shared publicationBing-Lin Sui
College of Chemistry and Chemical Engineering, Weifang University, Weifang, P. R. China
1 shared publicationBinglin Sui
College of Chemistry, Chemical and Environmental Engineering, Weifang University, No. 5147 Dongfeng Street, Weifang, 261061, P. R. China
1 shared publication
Latest Publications
- Top Cited PapersOpen Access
- 5 February 2026
- Published by Springer Nature in BMC Chemistry
- Vol. 20 (1)
Synthesis, structural characterization, DFT calculation, and antitumor activity of a new Co(II) complex based on 2-((2′-Carboxybenzyl)oxy)benzoic acid and 2,2′-bipyridine ligands
In this work, a new Co(II) complex, abbreviated as [Co(L)(bipy)(H2O)2]n (1) was prepared using cobalt(II) acetate tetrahydrate, 2-((2’-carboxybenzyl)
- 5 February 2026
- Published by Springer Nature in BMC Chemistry
- Vol. 20 (1)
Top Cited PapersOpen AccessSynthesis, structural characterization, DFT calculation, and antitumor activity of a new Co(II) complex based on 2-((2′-Carboxybenzyl)oxy)benzoic acid and 2,2′-bipyridine ligands
In this work, a new Co(II) complex, abbreviated as [Co(L)(bipy)(H2O)2]n (1) was prepared using cobalt(II) acetate tetrahydrate, 2-((2’-carboxybenzyl)
- Open Access
- 11 August 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 15 (35) , 28889-28896
A dual-type I/II NIR photosensitizer for effective cancer photodynamic therapy with enhanced ROS generation
Based on the cyanine dye scaffold, two photosensitizers (PSs) (C1 and C2) were successfully synthesized. These PSs exhibited a maximum absorption wavelength of 660 nm, falling within the near-infrared window. Compared to the commercially available photosensitizer ICG, the newly developed PSs demonstrated enhanced reactive oxygen species (ROS) generation under lower light doses. Notably, these PSs can simultaneously produce both singlet oxygen (1O2) and superoxide anion radicals (O2˙−), classifying them as dual type I/II PSs. Compared with C1, the 1O2 quantum yield of C2 was higher, as high as 10.6 times that of ICG. Theoretical calculations revealed that the molecules of C2 possessed a small singlet–triplet energy gap (ΔES–T), which facilitated more efficient intersystem crossing (ISC) from the singlet to triplet state, thereby promoting greater ROS generation. Experiments showed that C1 and C2 were located in mitochondria and could cause a decrease in mitochondrial membrane potential, leading to cell death. Animal experiments have shown that C2 effectively suppressed tumor growth without side effects.
- 11 August 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 15 (35) , 28889-28896
Open AccessA dual-type I/II NIR photosensitizer for effective cancer photodynamic therapy with enhanced ROS generation
Based on the cyanine dye scaffold, two photosensitizers (PSs) (C1 and C2) were successfully synthesized. These PSs exhibited a maximum absorption wavelength of 660 nm, falling within the near-infrared window. Compared to the commercially available photosensitizer ICG, the newly developed PSs demonstrated enhanced reactive oxygen species (ROS) generation under lower light doses. Notably, these PSs can simultaneously produce both singlet oxygen (1O2) and superoxide anion radicals (O2˙−), classifying them as dual type I/II PSs. Compared with C1, the 1O2 quantum yield of C2 was higher, as high as 10.6 times that of ICG. Theoretical calculations revealed that the molecules of C2 possessed a small singlet–triplet energy gap (ΔES–T), which facilitated more efficient intersystem crossing (ISC) from the singlet to triplet state, thereby promoting greater ROS generation. Experiments showed that C1 and C2 were located in mitochondria and could cause a decrease in mitochondrial membrane potential, leading to cell death. Animal experiments have shown that C2 effectively suppressed tumor growth without side effects.
- Open Access
- 24 June 2024
- Published by MDPI AG in Pharmaceuticals
- Vol. 17 (7) , 828
Comparative Efficacy and Safety of Glucagon-like Peptide-1 Receptor Agonists in Children and Adolescents with Obesity or Overweight: A Systematic Review and Network Meta-Analysis
Four glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have been used in children and adolescents with obesity or overweight. This network meta-analysis was conducted to compare the efficacy and safety of these regimens. Embase, PubMed, and Scopus were searched on March 2023 and updated in June 2024 for eligible randomized controlled trials (RCTs). The primary efficacy outcomes were mean difference in actual body weight, BMI (body mass index), BMI z score, and waist circumference. Safety outcomes included nausea, vomiting, diarrhea, abdominal pain, injection-site reaction, and hypoglycemia. Eleven RCTs with 953 participants were eligible. Semaglutide exhibited greater effects in reducing weight, BMI, and BMI z score versus the placebo. Semaglutide was associated with greater weight loss and BMI z score reduction in comparison with exenatide, liraglutide, and dulaglutide. Semaglutide also significantly decreased BMI than exenatide. None of the four GLP-1 RAs were associated with higher risks of diarrhea, headache, and abdominal pain versus the placebo. Liraglutide was more likely to cause nausea, vomiting, hypoglycemia, and injection-site reactions than the placebo. Liraglutide also had higher odds of causing injection-site reactions than other GLP-1 RAs. Semaglutide appeared to be the most effective and safe option among four GLP-1 RAs in children and adolescents with obesity or overweight.
- 24 June 2024
- Published by MDPI AG in Pharmaceuticals
- Vol. 17 (7) , 828
Open AccessComparative Efficacy and Safety of Glucagon-like Peptide-1 Receptor Agonists in Children and Adolescents with Obesity or Overweight: A Systematic Review and Network Meta-Analysis
Four glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have been used in children and adolescents with obesity or overweight. This network meta-analysis was conducted to compare the efficacy and safety of these regimens. Embase, PubMed, and Scopus were searched on March 2023 and updated in June 2024 for eligible randomized controlled trials (RCTs). The primary efficacy outcomes were mean difference in actual body weight, BMI (body mass index), BMI z score, and waist circumference. Safety outcomes included nausea, vomiting, diarrhea, abdominal pain, injection-site reaction, and hypoglycemia. Eleven RCTs with 953 participants were eligible. Semaglutide exhibited greater effects in reducing weight, BMI, and BMI z score versus the placebo. Semaglutide was associated with greater weight loss and BMI z score reduction in comparison with exenatide, liraglutide, and dulaglutide. Semaglutide also significantly decreased BMI than exenatide. None of the four GLP-1 RAs were associated with higher risks of diarrhea, headache, and abdominal pain versus the placebo. Liraglutide was more likely to cause nausea, vomiting, hypoglycemia, and injection-site reactions than the placebo. Liraglutide also had higher odds of causing injection-site reactions than other GLP-1 RAs. Semaglutide appeared to be the most effective and safe option among four GLP-1 RAs in children and adolescents with obesity or overweight.
- 18 August 2023
- Published by Elsevier in Clinical Nutrition
- Vol. 42 (10) , 1817-1826
Efficacy and safety of probiotics and synbiotics for functional constipation in children: A systematic review and meta-analysis of randomized clinical trials
- 18 August 2023
- Published by Elsevier in Clinical Nutrition
- Vol. 42 (10) , 1817-1826
Efficacy and safety of probiotics and synbiotics for functional constipation in children: A systematic review and meta-analysis of randomized clinical trials