Disease mechanisms and translational barriers guide nanocarrier design for nose to brain delivery in Alzheimer’s disease
Source abstract
Abstract
Alzheimer's disease (AD) is a progressive neurodegenerative disorder with limited disease-modifying treatment options, partly because many therapeutic agents show insufficient brain exposure and dose-limiting systemic adverse effects after conventional administration. Nose-to-brain (N2B) delivery has emerged as a non-invasive strategy to transport therapeutics to the central nervous system through the olfactory and trigeminal pathways, thereby partially bypassing the blood-brain barrier. Recent advances in nanomedicine and biomaterial engineering have further improved this approach by enhancing drug stability, nasal residence, mucosal transport, and brain-targeting efficiency. This review examines nanocarrier-enabled N2B delivery strategies for AD from a mechanism-guided perspective, highlighting how AD-related pathological processes shape the selection of therapeutic cargos and formulation designs. We discuss recent progress in the intranasal delivery of repurposed small molecules, natural products, insulin-related agents, peptides and proteins, extracellular vesicles, antibodies, and nucleic acid-based therapeutics. We further summarize major nanocarrier and formulation platforms, including lipid-based systems, polymeric nanoparticles, micelles, extracellular vesicles, in situ gels, and device-assisted delivery technologies. Particular attention is given to the design parameters that influence N2B performance, including particle size distribution/PDI, surface charge, mucus interaction, cargo protection, targeting modification, biodistribution, and deposition reproducibility. Finally, we critically evaluate the translational challenges that continue to limit clinical application, including species differences in nasal anatomy, dose-volume restrictions, device-dependent variability, limited human pharmacokinetic evidence, manufacturing complexity, long-term safety, and regulatory requirements. By integrating disease mechanisms, nanocarrier design, and translational considerations, this review provides a structured perspective for developing more rational and clinically feasible N2B nanodelivery systems for AD.
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References (100+)
Show source-provided references
1. Serrano-Pozo A, Escott-Price V, Grinberg LT, Pascoal T, Suarez-Calvet M, Dubois B, et al. Alzheimer’s disease. Lancet (London England). 2026;407(10544):2241–62.10.1016/S0140-6736(26)00198-4 ↗
2. Estimation of the global prevalence of dementia. in 2019 and forecasted prevalence in 2050: an analysis for the Global Burden of Disease Study 2019. Lancet Public health. 2022;7(2):e105–25.10.1016/S2468-2667(21)00249-8 ↗
3. 2024 Alzheimer’s disease facts and figures. Alzheimer’s & dementia: the journal of the Alzheimer’s Association. 2024;20(5):3708 – 821.10.1002/alz.13809 ↗
4. Passeri E, Elkhoury K, Morsink M, Broersen K, Linder M, Tamayol A, et al. Alzheimer’s disease: treatment strategies and their limitations. Int J Mol Sci. 2022;23(22):13954.10.3390/ijms232213954 ↗
5. Chamorro LB, Zulli B, Barone E. Insulin resistance: fueling oxidative stress and neurodegeneration. J Neural Transm. 2025;132(10):1567–86.10.1007/s00702-025-02956-6 ↗
6. D’Alessandro MCB, Kanaan S, Geller M, Praticò D, Daher JPL. Mitochondrial dysfunction in Alzheimer’s disease. Ageing Res Rev. 2025;107:102713.10.1016/j.arr.2025.102713 ↗
7. Wu X, Zang R, Qiu Y, Zhang Y, Peng J, Cheng Z, et al. Intranasal drug delivery technology in the treatment of central nervous system diseases: challenges, advances, and future research directions. Pharmaceutics. 2025;17(6):775.10.3390/pharmaceutics17060775 ↗
8. Abbott NJ, Patabendige AA, Dolman DE, Yusof SR, Begley DJ. Structure and function of the blood-brain barrier. Neurobiol Dis. 2010;37(1):13–25.10.1016/j.nbd.2009.07.030 ↗
9. Drath I, Richter F, Feja M. Nose-to-brain drug delivery: from bench to bedside. Translational neurodegeneration. 2025;14(1):23.10.1186/s40035-025-00481-w ↗
10. Lochhead JJ, Kellohen KL, Ronaldson PT, Davis TP. Distribution of insulin in trigeminal nerve and brain after intranasal administration. Sci Rep. 2019;9(1):2621.10.1038/s41598-019-39191-5 ↗
11. Thorne RG, Pronk GJ, Padmanabhan V, Frey WH 2. Delivery of insulin-like growth factor-I to the rat brain and spinal cord along olfactory and trigeminal pathways following intranasal administration. Neuroscience. 2004;127(2):481–96.10.1016/j.neuroscience.2004.05.029 ↗
12. Zhang Y, Liu M, Wang Y, Hu D, Wu S, Zhao B, et al. Nasal nanotherapeutics for central nervous system disorders: Bridging the translational gap in central nervous system drug delivery. Eur J Pharmacol. 2025;1003:177958.10.1016/j.ejphar.2025.177958 ↗
13. Rajput A, Pingale P, Dhapte-Pawar V. Nasal delivery of neurotherapeutics via nanocarriers: Facets, aspects, and prospects. Front Pharmacol. 2022;13:979682.10.3389/fphar.2022.979682 ↗
14. Sugandhi VV, Gattu K, Mundrathi V, Khairnar R, Arshad T, Kumar S, et al. Intranasal delivery of rapamycin via brain-targeting polymeric micelles for Alzheimer’s disease treatment. Int J Pharm. 2025;683:126011.10.1016/j.ijpharm.2025.126011 ↗
15. Zakharova L, Gaynanova G, Vasilieva E, Vasileva L, Pavlov R, Kashapov R, et al. Recent nanoscale carriers for therapy of Alzheimer’s disease: current strategies and perspectives. Curr Med Chem. 2023;30(33):3743–74.10.2174/0929867330666221115103513 ↗
16. de la Monte SM. Conquering insulin network dysfunctions in Alzheimer’s disease: where are we today? J Alzheimer’s disease: JAD. 2024;101(s1):S317–43.10.3233/JAD-240069 ↗
17. Zhang D, Zhang W, Ming C, Gao X, Yuan H, Lin X, et al. P-tau217 correlates with neurodegeneration in Alzheimer’s disease, and targeting p-tau217 with immunotherapy ameliorates murine tauopathy. Neuron. 2024;112(10):1676–e9312.10.1016/j.neuron.2024.02.017 ↗
18. Gaikwad S, Puangmalai N, Sonawane M, Montalbano M, Price R, Iyer MS, et al. Nasal tau immunotherapy clears intracellular tau pathology and improves cognitive functions in aged tauopathy mice. Sci Transl Med. 2024;16(754):eadj5958.10.1126/scitranslmed.adj5958 ↗
19. Dourte M, Paître E, Bouchoucha M, Boyer E, Tomé SO, Doeraene E, et al. The olfactory epithelium: a critical gateway for pathological tau propagation and a target for mitigating tauopathy in the central nervous system. Acta Neuropathol. 2025;149(1):64.10.1007/s00401-025-02902-6 ↗
20. Wong CYJ, Baldelli A, Hoyos CM, Tietz O, Ong HX, Traini D. Insulin delivery to the brain via the nasal route: unraveling the potential for Alzheimer’s disease therapy. Drug Del Translat Res. 2024;14(7):1776–93.10.1007/s13346-024-01558-1 ↗
21. Hallschmid M. Intranasal insulin for Alzheimer’s disease. CNS Drugs. 2021;35(1):21–37.10.1007/s40263-020-00781-x ↗
22. Madhu LN, Kodali M, Upadhya R, Rao S, Somayaji Y, Attaluri S, et al. Extracellular vesicles from human-induced pluripotent stem cell-derived neural stem cells alleviate proinflammatory cascades within disease-associated microglia in Alzheimer’s disease. J Extracell vesicles. 2024;13(11):e12519.10.1002/jev2.12519 ↗
23. Lopes JR, Zhang X, Mayrink J, Tatematsu BK, Guo L, LeServe DS, et al. Nasal administration of anti-CD3 monoclonal antibody ameliorates disease in a mouse model of Alzheimer’s disease. Proc Natl Acad Sci USA. 2023;120(37):e2309221120.10.1073/pnas.2309221120 ↗
24. Kaluza M, Ksiazek-Winiarek D, Szpakowski P, Czpakowska J, Fijalkowska J, Glabinski A. Polyphenols in the central nervous system: cellular effects and liposomal delivery approaches. Int J Mol Sci. 2025;26(13):6477.10.3390/ijms26136477 ↗
25. Mustafa AM, Bastawesy GA, Hatem S, Moussa RA, Hal DM, Fawzy MH, et al. Polyphenolic protection: the role of mangiferin in mitigating neurodegeneration and neuroinflammation. Inflammopharmacology. 2025;33(8):4535–52.10.1007/s10787-025-01854-3 ↗
26. Cunha S, Forbes B, Sousa Lobo JM, Silva AC. Improving drug delivery for Alzheimer’s disease through nose-to-brain delivery using nanoemulsions, nanostructured lipid carriers (NLC) and in situ hydrogels. Int J Nanomed. 2021;16:4373–90.10.2147/IJN.S305851 ↗
27. Galushkin A, Gozes I. Intranasal NAP (Davunetide): Neuroprotection and circadian rhythmicity. Adv Drug Deliv Rev. 2025;220:115573.10.1016/j.addr.2025.115573 ↗
28. Bariviera JL, Ribeiro LR, Furian AF, Mello FK, Oliveira MS. Effects of intranasal antibodies on murine models of neurological disorders: a systematic review. Eur J Pharmacol. 2025;1003:177940.10.1016/j.ejphar.2025.177940 ↗
29. Li J, Peng H, Zhang W, Li M, Wang N, Peng C, et al. Enhanced nose-to-brain delivery of combined small interfering rnas using lesion-recognizing nanoparticles for the synergistic therapy of Alzheimer’s disease. ACS Appl Mater Interfaces. 2023;15(46):53177–88.10.1021/acsami.3c08756 ↗
30. Wu DD, Salah YA, Ngowi EE, Zhang YX, Khattak S, Khan NH, et al. Nanotechnology prospects in brain therapeutics concerning gene-targeting and nose-to-brain administration. iScience. 2023;26(8):107321.10.1016/j.isci.2023.107321 ↗
31. Rather HA, Almousa S, Craft S, Deep G. Therapeutic efficacy and promise of stem cell-derived extracellular vesicles in Alzheimer’s disease and other aging-related disorders. Ageing Res Rev. 2023;92:102088.10.1016/j.arr.2023.102088 ↗
32. Hua Z, Zhou N, Zhou Z, Fu Z, Guo R, Akogo HY, et al. Intranasal administration of stem cell derivatives for the treatment of AD animal models: a systematic review and meta-analysis. Stem Cell Res Ther. 2025;16(1):409.10.1186/s13287-025-04555-4 ↗
33. Goel H, Kalra V, Verma SK, Dubey SK, Tiwary AK. Convolutions in the rendition of nose to brain therapeutics from bench to bedside: Feats & fallacies. J controlled release: official J Controlled Release Soc. 2022;341:782–811.10.1016/j.jconrel.2021.12.009 ↗
34. Bolon M, Fieux M, Monge C, Richard S. Polymeric nanoparticles for efficient nose-to-brain delivery. Nanoscale. 2025;17(31):17947–79.10.1039/D5NR00870K ↗
35. Georgieva D, Nikolova D, Vassileva E, Kostova B. Chitosan-based nanoparticles for targeted nasal galantamine delivery as a promising tool in Alzheimer’s disease therapy. Pharmaceutics. 2023;15(3):829.10.3390/pharmaceutics15030829 ↗
36. Guo H, Wang G, Zhai Z, Huang J, Huang Z, Zhou Y, et al. Rivastigmine nasal spray for the treatment of Alzheimer’s disease: olfactory deposition and brain delivery. Int J Pharm. 2024;652:123809.10.1016/j.ijpharm.2024.123809 ↗
37. Sai KKS, Erichsen JM, Gollapelli KK, Krizan I, Miller M, Damuka N, et al. First-in-human positron emission tomography study of intranasal insulin in aging and MCI. Volume 11. New York, N Y): Alzheimer’s & dementia; 2025. p. e70123. 3.
38. Solingapuram Sai KK, Erichsen JM, Gollapelli KK, Krizan I, Miller M, Bansode A, et al. First biodistribution study of [68Ga]Ga-NOTA-insulin following intranasal administration in adult vervet monkeys. J Alzheimer’s disease: JAD. 2024;101(1):309–20.10.3233/JAD-240484 ↗
39. Smith K, Fan J, Marriner GA, Gerdes J, Kessler R, Zinn KR. Distribution of insulin in primate brain following nose-to-brain transport. Volume 10. Alzheimer’s & dementia; 2024. p. e12459. (New York, N Y). 1.10.1002/trc2.12459 ↗
40. Ruan S, Li J, Ruan H, Xia Q, Hou X, Wang Z, et al. Microneedle-mediated nose-to-brain drug delivery for improved Alzheimer’s disease treatment. J Controlled Release Soc. 2024;366:712–31.10.1016/j.jconrel.2024.01.013 ↗
41. Martínez-Ortíz D, Altshuler P, Martínez-Ortíz L, Rodríguez-de-Torner LA, Chávez-Linares O, Altshuler E. Nasal model experiments show that a collimated fluid delivers precise doses to the human olfactory cavity in the side-laying position. J Pharm Sci. 2024;113(8):2475–83.10.1016/j.xphs.2024.05.005 ↗
42. Perkušić M, Nižić Nodilo L, Ugrina I, Špoljarić D, Jakobušić Brala C, Pepić I, et al. Tailoring functional spray-dried powder platform for efficient donepezil nose-to-brain delivery. Int J Pharm. 2022;624:122038.10.1016/j.ijpharm.2022.122038 ↗
43. Wang JL, Dong YY, Liu PL, Liao XR, Qi LJ, Huang QY, et al. Dual-Targeting Protein-Based Delivery System for enhanced drug therapy of neurodegenerative disorders. ACS Appl bio Mater. 2025;8(6):4898–907.10.1021/acsabm.5c00267 ↗
44. Tuna RW, Achmad NA, Kurniawan I, Khairiyah, Asaf MB, Sapiun Z, et al. Development of thermosensitive mucoadhesive gel incorporated lipid microspheres of donepezil for enhanced nose-to-brain delivery. J biomaterials Sci Polym Ed. 2025;36(15):2159–86.10.1080/09205063.2025.2492455 ↗
45. Salem HF, Aboud HM, Abdellatif MM, Abou-Taleb HA. Nose-to-brain targeted delivery of donepezil hydrochloride via novel hyaluronic acid-doped nanotransfersomes for Alzheimer’s disease mitigation. J Pharm Sci. 2024;113(7):1934–45.
46. Handa M, Sanap SN, Bhatta RS, Patil GP, Palkhade R, Singh DP, et al. Simultaneous intranasal codelivery of donepezil and memantine in a nanocolloidal carrier: optimization, pharmacokinetics, and pharmacodynamics studies. Mol Pharm. 2023;20(9):4714–28.10.1021/acs.molpharmaceut.3c00454 ↗
47. Wang G, Duan X, Ouyang D, Zhou J, Zhang H, Ding Y. Nose-to-brain delivery of donepezil within a small dose improves bioavailability and efficacy for Alzheimer’s disease treatment. Asian J Pharm Sci. 2026;21(2):101130.
48. Suthar T, Maurya R, Sonwani A, Upadhayay P, Datusalia AK, Naqvi S, et al. Nose-to-brain delivery of donepezil hydrochloride via Oleic acid-conjugated PAMAM G4 dendrimers for the treatment of Alzheimer’s-like dementia. Mol Pharm. 2026;23(1):177–95.10.1021/acs.molpharmaceut.5c00761 ↗
49. Khan SA, Qamar Z, Kamboj S, Moonis M, Rai G, Dang S, et al. Nose to brain delivery of nanostructured lipid carriers loaded with rivastigmine and nilotinib for treating Alzheimer’s disease: preparation, cell line study, and in vivo evaluation. Discover nano. 2025;20(1):93.10.1186/s11671-025-04276-w ↗
50. Kalra V, Silakari O, Tiwary AK. Intranasal administration of in silico designed Rivastigmine mucoadhesive nanoparticles ameliorates scopolamine-induced Alzheimer’s symptoms in mice: Pharmacokinetic and pharmacodynamic evidences. Int J Pharm. 2025;677:125635.10.1016/j.ijpharm.2025.125635 ↗
51. Subhash Hinge N, Kathuria H, Monohar Pandey M. Rivastigmine-DHA ion-pair complex improved loading in hybrid nanoparticles for better amyloid inhibition and nose-to-brain targeting in Alzheimer’s. Eur J Pharm biopharmaceutics: official J Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik eV. 2023;190:131–49.10.1016/j.ejpb.2023.06.007 ↗
52. Lotfi M, Nakhlband A, Doustmihan A, Omidi Y, Fathi M, Adibkia K. Formulation and evaluation of in-situ forming poloxamer-based hydrogel containing thiolated chitosan nanoparticles as intranasal galantamine delivery system. Int J Biol Macromol. 2025;320(Pt 1):145647.10.1016/j.ijbiomac.2025.145647 ↗
53. Sadiq AH, Alam MJ, Begum F, Hasan M, Kristof J, Mamun MA, et al. Enhancing galantamine distribution in rat brain using microplasma-assisted nose-to-brain drug delivery. Int J Mol Sci. 2025;26(4):1710.10.3390/ijms26041710 ↗
54. ElMosbah DE, Khattab MS, Ibrahim MA, El-Asssal MI, Miniawy H. Preclinical efficacy of oral and nasal rivastigmine-loaded chitosan nano-particles on AlCl(3)-induced Alzheimer’s-like disease in rats. Inflammopharmacology. 2024;32(6):3943–52.10.1007/s10787-024-01541-9 ↗
55. El-Ganainy SO, Gowayed MA, Agami M, Mohamed P, Belal M, Farid RM, et al. Galantamine nanoparticles outperform oral galantamine in an Alzheimer’s rat model: pharmacokinetics and pharmacodynamics. Nanomed (London England). 2021;16(15):1281–96.10.2217/nnm-2021-0051 ↗
56. Kurtukova V, Aktas S, Pupure J, Narbute K, Muceniece R, Pilipenko V. Low-dose intranasal metformin exerts neuroprotective effects in a rat model of sporadic Alzheimer’s disease. Mol Neurobiol. 2025;62(10):13029–43.10.1007/s12035-025-05079-x ↗
57. Kazkayasi I, Telli G, Nemutlu E, Uma S. Intranasal metformin treatment ameliorates cognitive functions via insulin signaling pathway in ICV-STZ-induced mice model of Alzheimer’s disease. Life Sci. 2022;299:120538.10.1016/j.lfs.2022.120538 ↗
58. Gouveia F, Carona A, Lacerda M, Bicker J, Camins A, Teresa Cruz M, et al. Unveiling the potential of intranasal delivery of renin-angiotensin system drugs: Insights on the pharmacokinetics of irbesartan. Biochem Pharmacol. 2024;230(Pt 3):116616.10.1016/j.bcp.2024.116616 ↗
59. Gouveia F, Pérez MC, Bicker J, Silva A, Santos AE, Pereira CF, et al. Protective effects of irbesartan against neurodegeneration in APP/PS1 mice: Unraveling its triple anti-apoptotic, anti-inflammatory and anti-oxidant action. Volume 188. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie; 2025. p. 118167.10.1016/j.biopha.2025.118167 ↗
60. Gouveia F, Fonseca C, Silva A, Camins A, Teresa Cruz M, Ettcheto M, et al. Intranasal irbesartan reverts cognitive decline and activates the PI3K/AKT pathway in an LPS-induced neuroinflammation mice model. Int Immunopharmacol. 2024;128:111471.10.1016/j.intimp.2023.111471 ↗
61. Moubarak GA, Salama AH, Ali AA, Galal AF, Fouad SA, Eid HM. Intranasal delivery of chitosan-coated bilosomes for repurposing Olmesartan in Alzheimer’s disease therapy: Formulation, optimization, pharmacokinetic and pharmacodynamic evaluation. J Pharm Sci. 2026;115(5):104241.10.1016/j.xphs.2026.104241 ↗
62. Balki S, Gautam AS, Balaji PG, Yadav AK, Singh RK. Montelukast attenuated memory decline, neuroinflammatory and neurodegenerative biomarkers in Aβ(1–42) exposed model of alzheimer’s disease in mice. Psychopharmacology. 2025;243(3):601–21.10.1007/s00213-025-06865-0 ↗
63. Groo AC, Curel T, Malzert-Fréon A, Séguy L, Bento O, Corvaisier S, et al. Evidence from a mouse model supports repurposing an anti-asthmatic drug, bambuterol, against Alzheimer’s disease by administration through an intranasal route. Commun biology. 2025;8(1):155.10.1038/s42003-025-07599-7 ↗
64. Imtiaz A, Shimonaka S, Uddin MN, Elahi M, Ishiguro K, Hasegawa M, et al. Selection of lansoprazole from an FDA-approved drug library to inhibit the Alzheimer’s disease seed-dependent formation of tau aggregates. Front Aging Neurosci. 2024;16:1368291.10.3389/fnagi.2024.1368291 ↗
65. Wen MM, Ismail NIK, Nasra MMA, El-Kamel AH. Repurposing ibuprofen-loaded microemulsion for the management of Alzheimer’s disease: evidence of potential intranasal brain targeting. Drug Delivery. 2021;28(1):1188–203.10.1080/10717544.2021.1937383 ↗
66. Botan MVG, da Silva JB, Bruschi ML. Development of nanostructured environmentally responsive system containing hydroxypropyl methylcellulose for nose-to-brain administration of meloxicam. Int J Biol Macromol. 2024;262(Pt 1):130015.10.1016/j.ijbiomac.2024.130015 ↗
67. Akel H, Ismail R, Katona G, Sabir F, Ambrus R, Csóka I. A comparison study of lipid and polymeric nanoparticles in the nasal delivery of meloxicam: formulation, characterization, and in vitro evaluation. Int J Pharm. 2021;604:120724.10.1016/j.ijpharm.2021.120724 ↗
68. Feng Q, Zhang X, Zhao X, Liu J, Wang Q, Yao Y, et al. Intranasal delivery of pure nanodrug loaded liposomes for Alzheimer’s disease treatment by efficiently regulating microglial polarization. Small. 2024;20(50):e2405781.
69. Malaiya A, Kenwat R, Mamgain A, Nayak P, Parker A, Paliwal SR, et al. Intranasal resveratrol delivery to the brain with chitosan-decorated bovine serum albumin nanoparticles: advancing Alzheimer’s management in old female rats through QbD-based optimization, in vitro evaluation, and in vivo exploration. Int J Biol Macromol. 2025;311(Pt 1):143300.10.1016/j.ijbiomac.2025.143300 ↗
70. Fonseca-Santos B, Cazarin CA, da Silva PB, Dos Santos KP, da Rocha MCO, Bao SN, et al. Intranasal in situ gelling liquid crystal for delivery of resveratrol ameliorates memory and neuroinflammation in Alzheimer’s disease. Nanomedicine: Nanatechnol biology Med. 2023;51:102689.10.1016/j.nano.2023.102689 ↗
71. Satpathy B, Rajwar TK, Mishra A, Saha I, Rai VK, Sahoo RK, et al. Intra-nasal delivery of Quercetin-Loaded Nanostructured Lipid Carriers (NLCs) in the management of Alzheimer’s disease: formulation, in vitro and in vivo assessment. Mol Neurobiol. 2025;62(10):13182–209.10.1007/s12035-025-05137-4 ↗
72. Sonawane D, Pokharkar V. Quercetin-loaded nanostructured lipid carrier in situ gel for brain targeting through intranasal route: formulation, in vivo pharmacokinetic and pharmacodynamic studies. AAPS PharmSciTech. 2024;25(2):30.10.1208/s12249-024-02736-7 ↗
73. Mi X, Ruan X, Lin R, Huang S, Cai P, Chen X, et al. Intranasal administration of Ganoderma lucidum-derived exosome-like nanovesicles ameliorates cognitive impairment by reducing inflammation in a mouse model of Alzheimer’s disease. Front Pharmacol. 2025;16:1572771.10.3389/fphar.2025.1572771 ↗
74. Sirvi PK, Balaji PG, Kumar A, Alam MI, Sharma A, Das N, et al. Lactoferrin-anchored carboxymethyl pullulan-MgO nanocomposites for targeted delivery of trans-ferulic acid: physicochemical characterization, in vitro and ex vivo studies. ACS Appl bio Mater. 2025;8(7):5757–74.10.1021/acsabm.5c00482 ↗
75. Saini S, Sharma T, Jain A, Kaur H, Katare OP, Singh B. Systematically designed chitosan-coated solid lipid nanoparticles of ferulic acid for effective management of Alzheimer’s disease: a preclinical evidence. Colloids and surfaces B. Biointerfaces. 2021;205:111838.10.1016/j.colsurfb.2021.111838 ↗
76. Prabakaran A, Rakshit D, Patel I, Susanna KJ, Mishra A, Radhakrishnanand P, et al. Enhanced cognitive function in mice through intranasal delivery of sinapic acid via chitosan-coated solid lipid nanoparticles. Int J Pharm. 2025;675:125565.10.1016/j.ijpharm.2025.125565 ↗
77. Prabakaran A, Rakshit D, Patel I, Susanna KJ, Mishra A, Radhakrishnanand P, et al. Chitosan-coated nanostructured lipid carriers for intranasal delivery of sinapic acid in Abeta(1)(-)(42) induced C57BL/6 mice for Alzheimer’s disease treatment. Int J Biol Macromol. 2025;305(Pt 2):141136.10.1016/j.ijbiomac.2025.141136 ↗
78. Sun C, Sha S, Shan Y, Gao X, Li L, Xing C, et al. Intranasal delivery of BACE1 siRNA and berberine via engineered stem cell exosomes for the treatment of Alzheimer’s disease. Int J Nanomed. 2025;20:5873–91.10.2147/IJN.S506793 ↗
79. Bahndare S, Mathure D, Ranpise H, Salunke M, Awasthi R. Surface-modified liposomal in-situ nasal gel enhances brain targeting of berberine hydrochloride for Alzheimer’s therapy: optimization and in vivo studies. J Liposome Res. 2025;35(2):135–52.10.1080/08982104.2024.2431908 ↗
80. Chakraborty S, Karmakar V, Chatterjee K, Chatterjee A, Dwivedi M, Gorain B. Chitosan nanoparticle-mediated nose-to-brain delivery of naringenin: attenuating memory decline in experimental animals via behavioural assessment and modulation of biochemical parameters. Int J Biol Macromol. 2025;286:138336.10.1016/j.ijbiomac.2024.138336 ↗
81. Abbas H, Sayed NSE, Youssef N, Mousa PMEG, Fayez MR, AM. Novel luteolin-loaded chitosan decorated nanoparticles for brain-targeting delivery in a sporadic Alzheimer’s disease mouse model: focus on antioxidant, anti-inflammatory, and amyloidogenic pathways. Pharmaceutics. 2022;14(5):1003.10.3390/pharmaceutics14051003 ↗
82. Elsheikh MA, El-Feky YA, Al-Sawahli MM, Ali ME, Fayez AM, Abbas H. A Brain-targeted approach to ameliorate memory disorders in a sporadic Alzheimer’s disease mouse model via intranasal luteolin-loaded nanobilosomes. Pharmaceutics. 2022;14(3):576.10.3390/pharmaceutics14030576 ↗
83. Wu F, Huang M, Zuo X, Xie R, Liu J, Ke J, et al. Osthole/borneol thermosensitive gel via intranasal administration enhances intracerebral bioavailability to improve cognitive impairment in APP/PS1 transgenic mice. Front Pharmacol. 2023;14:1224856.10.3389/fphar.2023.1224856 ↗
84. Vasdev N, Handa M, Kesharwani P, Shukla R. Rosemary oil low energy nanoemulsion: optimization, microrheology, in silico, in vitro, and ex vivo characterization. J biomaterials Sci Polym Ed. 2022;33(15):1901–23.10.1080/09205063.2022.2088527 ↗
85. Long C, Han X, Yang Y, Li T, Zhou Q, Chen Q. Efficacy of intranasal insulin in improving cognition in mild cognitive impairment or dementia: a systematic review and meta-analysis. Front Aging Neurosci. 2022;14:963933.10.3389/fnagi.2022.963933 ↗
86. Kellar D, Register T, Lockhart SN, Aisen P, Raman R, Rissman RA, et al. Intranasal insulin modulates cerebrospinal fluid markers of neuroinflammation in mild cognitive impairment and Alzheimer’s disease: a randomized trial. Sci Rep. 2022;12(1):1346.10.1038/s41598-022-05165-3 ↗
87. Karimani F, Asgari Taei A, Kaveh N, Rabiei Ghahfarokhi M, Abolghasemi Dehaqani MR, Dargahi L. Hippocampal sharp-wave ripples and hippocampal-prefrontal synchrony regulate memory-enhancing effects of intranasal insulin in an STZ-induced Alzheimer’s model. Life Sci. 2024;357:123094.10.1016/j.lfs.2024.123094 ↗
88. Woodfield A, Gonzales T, Helmerhorst E, Laws S, Newsholme P, Porter T, et al. Current insights on the use of insulin and the potential use of insulin mimetics in targeting insulin signalling in Alzheimer’s disease. Int J Mol Sci. 2022;23(24):15811.10.3390/ijms232415811 ↗
89. Rosenbloom M, Barclay TR, Kashyap B, Hage L, O’Keefe LR, Svitak A, et al. A phase II, single-center, randomized, double-blind, placebo-controlled study of the safety and therapeutic efficacy of intranasal glulisine in amnestic mild cognitive impairment and probable mild Alzheimer’s disease. Drugs Aging. 2021;38(5):407–15.10.1007/s40266-021-00845-7 ↗
90. Nguyen V, Thomas P, Pemberton S, Babin A, Noonan C, Weaver R, et al. Central nervous system insulin signaling can influence the rate of insulin influx into brain. Fluids Barr CNS. 2023;20(1):28.10.1186/s12987-023-00431-6 ↗
91. Khan TTS, Wong CYJ, Sheikh Z, Fathi A, Maleknia S, Oveissi F et al. Repurposing insulin for Alzheimer’s disease treatment: intranasal delivery of a thermoresponsive nanocarrier-based insulin formulation to the brain. Drug delivery and translational research. 2026.10.1007/s13346-026-02146-1 ↗
92. Abdulhameed N, Babin A, Hansen K, Weaver R, Banks WA, Talbot K, et al. Comparing regional brain uptake of incretin receptor agonists after intranasal delivery in CD-1 mice and the APP/PS1 mouse model of Alzheimer’s disease. Alzheimers Res Ther. 2024;16(1):173.10.1186/s13195-024-01537-1 ↗
93. Nowell J, Blunt E, Gupta D, Edison P. Antidiabetic agents as a novel treatment for Alzheimer’s and Parkinson’s disease. Ageing Res Rev. 2023;89:101979.10.1016/j.arr.2023.101979 ↗
94. Vulih-Shultzman I, Pinhasov A, Mandel S, Grigoriadis N, Touloumi O, Pittel Z, et al. Activity-dependent neuroprotective protein snippet NAP reduces tau hyperphosphorylation and enhances learning in a novel transgenic mouse model. J Pharmacol Exp Ther. 2007;323(2):438–49.10.1124/jpet.107.129551 ↗
95. Gozes I, Blatt J, Lobyntseva A. Davunetide sex-dependently boosts memory in prodromal Alzheimer’s disease. Translation Psych. 2024;14(1):412.10.1038/s41398-024-03118-0 ↗
96. Hatakawa Y, Tanaka A, Furubayashi T, Katsumi H, Nakamura R, Konishi M, et al. Efficient nose-to-brain delivery of nine residues peptide (JAL-TA9) exhibiting hydrolytic activity against amyloid-beta. Eur J Pharm biopharmaceutics: official J Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik eV. 2025;208:114661.10.1016/j.ejpb.2025.114661 ↗
97. Hatakawa Y, Tanaka A, Furubayashi T, Nakamura R, Konishi M, Akizawa T, et al. Direct delivery of ANA-TA9, a peptide capable of Abeta hydrolysis, to the brain by intranasal administration. Pharmaceutics. 2021;13(10):1673.10.3390/pharmaceutics13101673 ↗
98. Li X, Liu C, Li W, Qi G, Dai Y, Gu C, et al. Multi-omics delineate growth factor network underlying exercise effects in an Alzheimer’s mouse model. Alzheimer’s Dement J Alzheimer’s Assoc. 2025;21(3):e70024.10.1002/alz.70024 ↗
99. Guo K, Huang W, Chen K, Huang P, Peng W, Shi R, et al. Fibroblast growth factor 10 ameliorates neurodegeneration in mouse and cellular models of Alzheimer’s disease via reducing tau hyperphosphorylation and neuronal apoptosis. Aging Cell. 2023;22(9):e13937.10.1111/acel.13937 ↗
100. Fitzgerald GS, Chuchta TG, McNay EC. Insulin-like growth factor-2 is a promising candidate for the treatment and prevention of Alzheimer’s disease. CNS Neurosci Ther. 2023;29(6):1449–69.10.1111/cns.14160 ↗