Microneedle Patch Prepared from a Hydrogel by a Mild Method for Insulin Delivery
Source abstract
Abstract
Abstract Most reported microneedle patches still suffer from a complicated preparation process and insufficient loading capacity for the glucose‐responsive delivery system. Herein, based on the reversibility of the boronate ester bond, a novel gel was formed by mixing phenylboronic acid grafted sodium hyaluronate and polyvinyl alcohol. The insulin‐loaded microneedle patch could be directly obtained by simply blending high‐dose insulin and gel into the mold. The introduction of cellulose nanofiber was also found to be in favor of mechanical strength. The glucose responsibility could be achieved when the boronate ester bond was broken by glucose, leading to the change of crosslinking density and further controlling insulin release. In the hypoglycemic experiment of diabetic rats, the microneedle patches could effectively puncture the skin and maintain normal blood glucose levels for an extended period. The facile preparation process and high loading capacity give this microneedle patch a great chance in mass production.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Transdermal Drug Delivery · Advanced Drug Delivery Systems · Lipid Membrane Structure and Behavior
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Engineering College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 P. R. China
The First Affiliated Hospital of Zhejiang University College of Medicine Zhejiang University Hangzhou 310027 P. R. China
Funding
Science and Technology Program of Zhejiang Province · Natural Science Foundation of Zhejiang Province
References (34)
Show source-provided references
1. InternationalDiabetesFederation IDF Diabetes atlas 9th edition 2019.https://www.idf.org/. Accessed August 2020.
2. 10.1039/C5RA04340A10.1039/C5RA04340A ↗
3. 10.1039/c3cs60436e10.1039/c3cs60436e ↗
4. 10.1016/j.jconrel.2018.08.04210.1016/j.jconrel.2018.08.042 ↗
5. 10.1073/pnas.150540511210.1073/pnas.1505405112 ↗
6.
7. 10.1021/acsnano.6b0689210.1021/acsnano.6b06892 ↗
8. 10.1039/C7TB02082A10.1039/C7TB02082A ↗
9. 10.1021/acs.nanolett.6b0384810.1021/acs.nanolett.6b03848 ↗
10. 10.1002/smll.20170418110.1002/smll.201704181 ↗
11. 10.1038/s41467-017-01764-110.1038/s41467-017-01764-1 ↗
12. Wang J. Q. · Sci. Adv. · 2019 · 5 · 10
13.
14. 10.1002/adfm.20180736910.1002/adfm.201807369 ↗
15. 10.1038/s41551-019-0508-y10.1038/s41551-019-0508-y ↗
16.
17. 10.1016/j.msec.2016.02.00510.1016/j.msec.2016.02.005 ↗
18. 10.1007/s00396-014-3490-710.1007/s00396-014-3490-7 ↗
19. 10.1016/j.carbpol.2019.11580310.1016/j.carbpol.2019.115803 ↗
20.
21. 10.1021/acs.iecr.0c0108310.1021/acs.iecr.0c01083 ↗
22. 10.1002/adfm.20150055410.1002/adfm.201500554 ↗
23. 10.1002/adma.20150290210.1002/adma.201502902 ↗
24.
25. 10.1021/acs.macromol.6b0144810.1021/acs.macromol.6b01448 ↗
26. 10.1016/S0032-3861(00)00627-310.1016/S0032-3861(00)00627-3 ↗
27. 10.1002/app.4942110.1002/app.49421 ↗
28. 10.1016/j.msec.2017.05.14310.1016/j.msec.2017.05.143 ↗
29.
30. 10.1002/anie.20110625210.1002/anie.201106252 ↗
31. 10.1002/ange.20110625210.1002/ange.201106252 ↗
32. 10.1021/bm034139o10.1021/bm034139o ↗
33. 10.1039/C4CC04760E10.1039/C4CC04760E ↗
34. 10.1021/ac970726m10.1021/ac970726m ↗