journal article·2025-10-02

Chitosan-based nanoparticles for perillyl alcohol delivery: development, cytotoxicity and mucoadhesion

Larissa Penteado, Thaysa Ksiaskiewcz Karam, Celso Vataru Nakamura, Rubiana Mara Mainardes

Soft Materials· Volume 23· Issue 3-4
Publisher page

Abstract

Perillyl alcohol (POH) is a monoterpene found in the essential oils of several plants and citrus fruits, with well-documented anticancer potential. However, its poor aqueous solubility and low oral bioavailability significantly limit its therapeutic efficacy. This study describes the development of mucoadhesive chitosan/tripolyphosphate (CS/TPP) nanoparticles for the encapsulation and controlled delivery of POH. The nanoparticles, prepared by ionic gelation, exhibited a mean diameter of ~300 nm, a positive zeta potential (+9 ± 3 mV), low polydispersity (0.09 ± 0.04), spherical morphology, and an encapsulation efficiency of 35 ± 3%. XRD and DSC analyses indicated partial amorphization and enhanced thermal stability of the encapsulated compound, whereas FTIR confirmed nanoparticle formation and suggested physical entrapment of POH within the chitosan matrix. The formulation provided sustained POH release for up to 144 h, with approximately 38% released over the first 72 h. Cytotoxicity assays in HT-29 and LNCaP cells demonstrated concentration-dependent reductions in viability for both free and encapsulated POH, with higher IC50 values for the nanoparticle formulation, consistent with its prolonged release profile. Mucoadhesion studies revealed significant mucin adsorption, physicochemical alterations upon contact with mucin, and clear evidence of surface interactions by SEM, supporting strong mucoadhesive properties. Collectively, these findings highlight CS/TPP/POH nanoparticles as a promising platform to improve the oral delivery, absorption, and therapeutic potential of POH for cancer treatment.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Drug Delivery Systems · Silymarin and Mushroom Poisoning · Advancements in Transdermal Drug Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Universidade Estadual do Centro-Oeste-UNICENTRO

Universidade Estadual de Maringá-UEM

Funding

Conselho Nacional de Desenvolvimento Científico eTecnológico · Coordenação de Aperfeiçoamento de Pessoal de Nível Superior · Fundação Araucária · Financiadora de Projetos eEstudos · COMCAP-UEM

References (47)

Show source-provided references
1. 10.1016/B978-0-12-802215-3.00002-110.1016/B978-0-12-802215-3.00002-1 ↗
2. 10.3390/pharmaceutics1312216710.3390/pharmaceutics13122167 ↗
3. 10.1016/j.phymed.2024.15582610.1016/j.phymed.2024.155826 ↗
4. 10.3390/cancers1623400310.3390/cancers16234003 ↗
5. 10.1016/j.jprot.2010.01.00310.1016/j.jprot.2010.01.003 ↗
6. Clark, S. S., Zhong, L., Filiault, D., Perman, S., Ren, Z., Gould, M., and Yang, X. Anti-Leukemia Effect of Perillyl Alcohol in BCR/ABL-Transformed Cells Indirectly Inhibits Signaling Through MEK in a Ras- and Raf-Independent Fashion. Clin. Cancer Res. Oct 1, 2003, 9(12), 4494–4504.
7. 10.3390/ijms1912390510.3390/ijms19123905 ↗
8. 10.1016/j.intimp.2016.06.03410.1016/j.intimp.2016.06.034 ↗
9. 10.2174/187152061766617010309392310.2174/1871520617666170103093923 ↗
10. 10.1016/j.surneu.2007.07.04010.1016/j.surneu.2007.07.040 ↗
11. 10.1007/s00432-010-0873-010.1007/s00432-010-0873-0 ↗
12. 10.1007/s00280-007-0585-610.1007/s00280-007-0585-6 ↗
13. 10.1186/s12885-020-06802-810.1186/s12885-020-06802-8 ↗
14. 10.1016/j.addr.2012.09.01510.1016/j.addr.2012.09.015 ↗
15. 10.1039/C6NR03256G10.1039/C6NR03256G ↗
16. 10.3390/md1812060510.3390/md18120605 ↗
17. 10.1007/s10973-022-11909-010.1007/s10973-022-11909-0 ↗
18. 10.1016/j.jconrel.2004.08.01010.1016/j.jconrel.2004.08.010 ↗
19. 10.3390/molecules2804196310.3390/molecules28041963 ↗
20. 10.3390/ijms2404329310.3390/ijms24043293 ↗
21. 10.1038/s41598-022-23386-410.1038/s41598-022-23386-4 ↗
22. 10.1016/j.foodhyd.2016.08.02010.1016/j.foodhyd.2016.08.020 ↗
23. 10.1016/j.carbpol.2013.02.03110.1016/j.carbpol.2013.02.031 ↗
24. 10.3390/ph1608105510.3390/ph16081055 ↗
25. 10.1002/bmc.503710.1002/bmc.5037 ↗
26. 10.1080/1539445X.2021.190670210.1080/1539445X.2021.1906702 ↗
27. 10.1021/acsnanoscienceau.4c0005710.1021/acsnanoscienceau.4c00057 ↗
28. 10.1007/s00396005005010.1007/s003960050050 ↗
29. 10.1016/j.colsurfb.2011.09.04210.1016/j.colsurfb.2011.09.042 ↗
30. 10.1002/bit.2236310.1002/bit.22363 ↗
31. 10.1007/s12668-024-01614-710.1007/s12668-024-01614-7 ↗
32. 10.1016/j.ijbiomac.2015.08.01010.1016/j.ijbiomac.2015.08.010 ↗
33. 10.1016/j.lwt.2016.02.03710.1016/j.lwt.2016.02.037 ↗
34. 10.1080/01496395.2018.148984510.1080/01496395.2018.1489845 ↗
35. Chandra Dey, S., Al-Amin, M., Ur Rashid, T., Zakir Sultan, M., Ashaduzzaman, M., Sarker, M. and Md Shamsuddin, S. Preparation, Characterization and Performance Evaluation of Chitosan as an Adsorbent for Remazol Red. Int. J. Latest Res. Eng. Technol. 2016, 2(21), 52–62.
36. 10.1016/j.carbpol.2010.02.02610.1016/j.carbpol.2010.02.026 ↗
37. 10.1016/j.carbpol.2006.02.00810.1016/j.carbpol.2006.02.008 ↗
38. 10.1016/j.jddst.2015.04.00710.1016/j.jddst.2015.04.007 ↗
39. 10.1016/j.ijpharm.2011.03.05110.1016/j.ijpharm.2011.03.051 ↗
40. 10.1016/0168-3659(87)90035-610.1016/0168-3659(87)90035-6 ↗
41. 10.1385/IJGC:32:2-3:12510.1385/IJGC:32:2-3:125 ↗
42. 10.1016/j.ejpb.2015.05.00410.1016/j.ejpb.2015.05.004 ↗
43. 10.1208/pt05046710.1208/pt050467 ↗
44. 10.3109/10837450.2011.64068810.3109/10837450.2011.640688 ↗
45. 10.1016/j.foodhyd.2019.03.04210.1016/j.foodhyd.2019.03.042 ↗
46. 10.1016/j.ijbiomac.2021.01.04110.1016/j.ijbiomac.2021.01.041 ↗
47. 10.1016/j.ejpb.2015.03.02710.1016/j.ejpb.2015.03.027 ↗