Show source-provided references
1. Bannuru, RR, Schmid, CH, Kent, DM, Vaysbrot, EE, Wong, JB, McAlindon, TE. Comparative effectiveness of pharmacologic interventions for knee osteoarthritis: a systematic review and network meta-analysis. Ann Intern Med 2015;162:46–54. https://doi.org/10.7326/m14-1231.
10.7326/M14-1231 ↗2. Mora, JC, Przkora, R, Cruz-Almeida, Y. Knee osteoarthritis: pathophysiology and current treatment modalities. J Pain Res 2018;5:2189–96. https://doi.org/10.2147/jpr.s154002.
10.2147/JPR.S154002 ↗3. Sharma, V, Anuvat, K, John, L, Davis, M. Scientific American pain management-arthritis of the knee. Decker: pain related disease states. 2017.
10.2310/PM.15056 ↗4. Kellgren, JH, Lawrence, JS. Radiological assessment of osteo-arthrosis. Ann Rheum Dis 1957;16:494–502. https://doi.org/10.1136/ard.16.4.494.
10.1136/ard.16.4.494 ↗5. Richards, MM, Maxwell, JS, Weng, L, Angelos, MG, Golzarian, J. Intra-articular treatment of knee osteoarthritis: from anti-inflammatories to products of regenerative medicine. Physician Sportsmed 2016;44:101–8. https://doi.org/10.1080/00913847.2016.1168272.
10.1080/00913847.2016.1168272 ↗6. Chen, DI, Shen, J, Zhao, W, Wang, T, Han, L, Hamilton, JL, et al.. Osteoarthritis: toward a comprehensive understanding of pathological mechanism. Bone Res 2017;5:1–3. https://doi.org/10.1038/boneres.2016.44.
10.1038/boneres.2016.44 ↗7. Felson, DT, Naimark, A, Anderson, J, Kazis, L, Castelli, W, Meenan, RF. The prevalence of knee osteoarthritis in the elderly. The framingham osteoarthritis study. Arthritis Rheum Off J Am Coll Rheumatol 1987;30:914–8. https://doi.org/10.1002/art.1780300811.
10.1002/art.1780300811 ↗8. Jordan, JM, Helmick, CG, Renner, JB, Luta, G, Dragomir, AD, Woodard, J, et al.. Prevalence of knee symptoms and radiographic and symptomatic knee osteoarthritis in African Americans and Caucasians: the Johnston County Osteoarthritis Project. J Rheumatol 2007;34:172–80.
9. Dillon, CF, Rasch, EK, Gu, Q, Hirsch, R. Prevalence of knee osteoarthritis in the United States: arthritis data from the third national health and Nutrition Examination Survey 1991-94. J Rheumatol 2006;33:2271–9.
10. Loeser, RF. Aging and osteoarthritis. Curr Opin Rheumatol 2011;23:492–6. https://doi.org/10.1097/bor.0b013e3283494005.
10.1097/BOR.0b013e3283494005 ↗11. Kim, J, Xu, M, Xo, R, Mates, A, Wilson, GL, Pearsall, IVAW, et al.. Mitochondrial DNA damage is involved in apoptosis caused by pro-inflammatory cytokines in human OA chondrocytes. Osteoarthr Cartil 2010;18:424–32. https://doi.org/10.1016/j.joca.2009.09.008.
10.1016/j.joca.2009.09.008 ↗12. Goodwin, W, McCabe, D, Sauter, E, Reese, E, Walter, M, Buckwalter, JA, et al.. Rotenone prevents impact‐induced chondrocyte death. J Orthop Res 2010;28:1057–63. https://doi.org/10.1002/jor.21091.
10.1002/jor.21091 ↗13. Xia, B, Chen, D, Zhang, J, Hu, S, Jin, H, Tong, P. Osteoarthritis pathogenesis: a review of molecular mechanisms. Calcif Tissue Int 2014;95:495–505. https://doi.org/10.1007/s00223-014-9917-9.
10.1007/s00223-014-9917-9 ↗14. Goldring, MB, Goldring, SR. Articular cartilage and subchondral bone in the pathogenesis of osteoarthritis. Ann N Y Acad Sci 2010;1192:230–7. https://doi.org/10.1111/j.1749-6632.2009.05240.x.
10.1111/j.1749-6632.2009.05240.x ↗15. Mort, JS, Billington, CJ. Articular cartilage and changes in arthritis: matrix degradation. Arthritis Res Ther 2001;3:1–5.
10.1186/ar325 ↗16. Km, C. Gene deletion of either IL-1β, IL-1β-converting enzyme, inducible nitric oxide synthase, or stromelysin 1 accelerates the development of knee osteoarthritis in mice after surgical transection of the medial collateral ligament and partial medial meniscectomy. Arthritis Rheum 2003;48:3452–63.
10.1002/art.11355 ↗17. Li, Y, Xu, L, Olsen, BR. Lessons from genetic forms of osteoarthritis for the pathogenesis of the disease. Osteoarthr Cartil 2007;15:1101–5. https://doi.org/10.1016/j.joca.2007.04.013.
10.1016/j.joca.2007.04.013 ↗18. Kannu, P, Bateman, JF, Belluoccio, D, Fosang, AJ, Savarirayan, R. Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis. Arthritis Rheum Off J Am Coll Rheumatol 2009;60:325–34. https://doi.org/10.1002/art.24251.
10.1002/art.24251 ↗19. van der Kraan, PM, Goumans, MJ, Blaney Davidson, E, Ten Dijke, P. Age-dependent alteration of TGF-β signalling in osteoarthritis. Cell Tissue Res 2012;347:257–65. https://doi.org/10.1007/s00441-011-1194-6.
10.1007/s00441-011-1194-6 ↗20. Kolpakova, E, Olsen, BR. Wnt/β-catenin – a canonical tale of cell-fate choice in the vertebrate skeleton. Dev Cell 2005;8:626–7. https://doi.org/10.1016/j.devcel.2005.04.008.
10.1016/j.devcel.2005.04.008 ↗21. Degnin, CR, Laederich, MB, Horton, WA. FGFs in endochondral skeletal development. J Cell Biochem 2010;110:1046–57. https://doi.org/10.1002/jcb.22629.
10.1002/jcb.22629 ↗22. Schmidt, MB, Chen, EH, Lynch, SE. A review of the effects of insulin-like growth factor and platelet derived growth factor on in vivo cartilage healing and repair. Osteoarthr Cartil 2006;14:403–12. https://doi.org/10.1016/j.joca.2005.10.011.
10.1016/j.joca.2005.10.011 ↗23. Davidson, EB, Vitters, EL, Van Der Kraan, PM, Van, DBWB. Expression of transforming growth factor-β (TGFβ) and the TGFβ signalling molecule SMAD-2P in spontaneous and instability-induced osteoarthritis: role in cartilage degradation, chondrogenesis and osteophyte formation. Ann Rheum Dis 2006;65:1414–21. https://doi.org/10.1136/ard.2005.045971.
10.1136/ard.2005.045971 ↗24. Zhen, G, Wen, C, Jia, X, Li, Y, Crane, JL, Mears, SC, et al.. Inhibition of TGF-β signaling in mesenchymal stem cells of subchondral bone attenuates osteoarthritis. Nat Med 2013;19:704–12. https://doi.org/10.1038/nm.3143.
10.1038/nm.3143 ↗25. Fortier, LA, Barker, JU, Strauss, EJ, McCarrel, TM, Cole, BJ. The role of growth factors in cartilage repair. Clin Orthop Relat Res® 2011;469:2706–15. https://doi.org/10.1007/s11999-011-1857-3.
10.1007/s11999-011-1857-3 ↗26. Chia, SL, Sawaji, Y, Burleigh, A, McLean, C, Inglis, J, Saklatvala, J, et al.. Fibroblast growth factor 2 is an intrinsic chondroprotective agent that suppresses ADAMTS‐5 and delays cartilage degradation in murine osteoarthritis. Arthritis Rheum off J Am Coll Rheumatol 2009;60:2019–27. https://doi.org/10.1002/art.24654.
10.1002/art.24654 ↗27. Cucchiarini, M, Terwilliger, EF, Kohn, D, Madry, H. Remodelling of human osteoarthritic cartilage by FGF‐2, alone or combined with Sox9 via rAAV gene transfer. J Cell Mol Med 2009;13:2476–88. https://doi.org/10.1111/j.1582-4934.2008.00474.x.
10.1111/j.1582-4934.2008.00474.x ↗28. Lee, AS, Ellman, MB, Yan, D, Kroin, JS, Cole, BJ, van Wijnen, AJ, et al.. A current review of molecular mechanisms regarding osteoarthritis and pain. Gene 2013;527:440–7. https://doi.org/10.1016/j.gene.2013.05.069.
10.1016/j.gene.2013.05.069 ↗29. Ghosh, P. The pathobiology of osteoarthritis and the rationale for the use of pentosan polysulfate for its treatment. InSeminars Arthritis Rheum 1999;28:211–67. https://doi.org/10.1016/s0049-0172(99)80021-3.
10.1016/S0049-0172(99)80021-3 ↗30. Evans, CH, Watkins, SC, Stefanović-Račić, M. Nitric oxide and cartilage metabolism. Methods Enzymol 1996;269:75–88. https://doi.org/10.1016/s0076-6879(96)69011-9.
10.1016/S0076-6879(96)69011-9 ↗31. Ghosh, P, Smith, M. Osteoarthritis, genetic and molecular mechanisms. Biogerontology 2002;3:85–8. https://doi.org/10.1023/a:1015219716583.
10.1023/A:1015219716583 ↗32. Zhang, Y, McAlindon, TE, Hannan, MT, Chaisson, CE, Klein, R, Wilson, PW, et al.. Estrogen replacement therapy and worsening of radiographic knee osteoarthritis: the Framingham study. Arthritis Rheum Off J Am Coll Rheumatol 1998;41:1867–73. https://doi.org/10.1002/1529-0131(199810)41:10<1867::aid-art20>3.3.co;2-n.
10.1002/1529-0131(199810)41:10<1867::AID-ART20>3.3.CO;2-N ↗33. Nevitt, MC, Lane, NE, Scott, JC, Hochberg, MC, Pressman, AR, Genant, HK, et al.. Radiographic osteoarthritis of the hip and bone mineral density. Arthritis Rheum Off J Am Coll Rheumatol 1995;38:907–16. https://doi.org/10.1002/art.1780380706.
10.1002/art.1780380706 ↗34. Felson, DT, Zhang, Y, Anthony, JM, Naimark, A, Anderson, JJ. Weight loss reduces the risk for symptomatic knee osteoarthritis in women: the framingham study. Ann Intern Med 1992;116:535–9. https://doi.org/10.7326/0003-4819-116-7-535.
10.7326/0003-4819-116-7-535 ↗35. Kohatsu, N, Schurman, D. Risk factors for the development of osteoarthrosis of the knee. Clin Orthop Relat Res 1990;261:242–6. https://doi.org/10.1097/00003086-199012000-00028.
10.1097/00003086-199012000-00028 ↗36. Kivitz, A, Eisen, G, Zhao, WW, Bevirt, T, Recker, DP. Randomized placebo-controlled trial comparing efficacy and safety of valdecoxib with naproxen in patients with osteoarthritis. J Fam Pract 2002;51:530–7.
37. Dingle, JT. The effects of NSAID on the matrix of human articular cartilages. Z Rheumatol 1999;58:125–9. https://doi.org/10.1007/s003930050161.
10.1007/s003930050161 ↗38. El, HH, Marcelis, A, Devogelaer, JP, Manicourt, DH. Celecoxib has a positive effect on the overall metabolism of hyaluronan and proteoglycans in human osteoarthritic cartilage. J Rheumatol 2003;30:2444–51.
39. Yang, KA, Saris, DB, Dhert, WJ, Verbout, AJ. Osteoarthritis of the knee: current treatment options and future directions. Curr Orthop 2004;18:311–20. https://doi.org/10.1016/j.cuor.2004.04.005.
10.1016/j.cuor.2004.04.005 ↗40. Balazs, EA, Denlinger, JL. Viscosupplementation: a new concept in the treatment of osteoarthritis. J Rheumatol. Supplement 1993;39:3–9.
41. Leopold, SS, Redd, BB, Warme, WJ, Wehrle, PA, Pettis, PD, Shott, S. Corticosteroid compared with hyaluronic acid injections for the treatment of osteoarthritis of the knee: a prospective, randomized trial. JBJS 2003;85:1197–203. https://doi.org/10.2106/00004623-200307000-00003.
10.2106/00004623-200307000-00003 ↗42. Leardini, G, Mattara, L, Franceschini, M, Perbellini, A. Intra-articular treatment of knee osteoarthritis. A comparative study between hyaluronic acid and 6-methyl prednisolone acetate. Clin Exp Rheumatol 1991;9:375–81.
43. Jackson, DW, Evans, NA, Thomas, BM. Accuracy of needle placement into the intra-articular space of the knee. JBJS 2002;84:1522–7. https://doi.org/10.2106/00004623-200209000-00003.
10.2106/00004623-200209000-00003 ↗44. Steadman, JR, Briggs, KK, Rodrigo, JJ, Kocher, MS, Gill, TJ, Rodkey, WG. Outcomes of microfracture for traumatic chondral defects of the knee: average 11-year follow-up. Arthrosc J Arthrosc Relat Surg 2003;19:477–84. https://doi.org/10.1053/jars.2003.50112.
10.1053/jars.2003.50112 ↗45. Peterson, L, Minas, T, Brittberg, M, Nilsson, A, Sjögren-Jansson, E, Lindahl, A. Two-to 9-year outcome after autologous chondrocyte transplantation of the knee. Clin Orthop Relat Res 2000;374:212–34. https://doi.org/10.1097/00003086-200005000-00020.
10.1097/00003086-200005000-00020 ↗46. Bentley, G, Biant, LC, Carrington, RW, Akmal, M, Goldberg, A, Williams, AM, et al.. A prospective, randomised comparison of autologous chondrocyte implantation versus mosaicplasty for osteochondral defects in the knee. J Bone Jt Surg Br 2003;85:223–30. https://doi.org/10.1302/0301-620x.85b2.13543.
10.1302/0301-620X.85B2.13543 ↗47. Richard, MJ, Driban, JB, McAlindon, TE. Pharmaceutical treatment of osteoarthritis. Osteoarthr Cartil 2023;31:458–66. https://doi.org/10.1016/j.joca.2022.11.005.
10.1016/j.joca.2022.11.005 ↗48. Scott, PA, Kingsley, GH, Smith, CM, Choy, EH, Scott, DL. Non-steroidal anti-inflammatory drugs and myocardial infarctions: comparative systematic review of evidence from observational studies and randomised controlled trials. Ann Rheum Dis 2007;66:1296–304. https://doi.org/10.1136/ard.2006.068650.
10.1136/ard.2006.068650 ↗49. Ioannidis, JP, Haidich, AB, Pappa, M, Pantazis, N, Kokori, SI, Tektonidou, MG, et al.. Comparison of evidence of treatment effects in randomized and nonrandomized studies. JAMA 2001;286:821–30. https://doi.org/10.1001/jama.286.7.821.
10.1001/jama.286.7.821 ↗50. Cooper, C, Chapurlat, R, Al-Daghri, N, Herrero-Beaumont, G, Bruyère, O, Rannou, F, et al.. Safety of oral non-selective non-steroidal anti-inflammatory drugs in osteoarthritis: what does the literature say? Drugs Aging 2019;36:15–24. https://doi.org/10.1007/s40266-019-00660-1.
10.1007/s40266-019-00660-1 ↗51. Kolasinski, SL, Neogi, T, Hochberg, MC, Oatis, C, Guyatt, G, Block, J, et al.. American College of Rheumatology/Arthritis Foundation guideline for the management of osteoarthritis of the hand, hip, and knee. Arthritis Rheumatol 2020;72:220–33. https://doi.org/10.1002/art.41142.
10.1002/art.41142 ↗52. Dajani, EZ, Islam, K. Cardiovascular and gastrointestinal toxicity of selective cyclo-oxygenase-2 inhibitors in man. J Physiol Pharmacol 2008;59:117–33.
53. Harris, RC, Breyer, MD. Update on cyclooxygenase-2 inhibitors. Clin J Am Soc Nephrol 2006;1:236–45. https://doi.org/10.2215/cjn.00890805.
10.2215/CJN.00890805 ↗54. Kijowski, R. Risks and benefits of intra-articular corticosteroid injection for treatment of osteoarthritis: what radiologists and patients need to know. Radiology 2019;293:664–5. https://doi.org/10.1148/radiol.2019192034.
10.1148/radiol.2019192034 ↗55. McAlindon, TE, LaValley, MP, Harvey, WF, Price, LL, Driban, JB, Zhang, M, et al.. Effect of intra-articular triamcinolone vs saline on knee cartilage volume and pain in patients with knee osteoarthritis: a randomized clinical trial. JAMA 2017;317:1967–75. https://doi.org/10.1001/jama.2017.5283.
10.1001/jama.2017.5283 ↗56. Anand, P, Bley, K. Topical capsaicin for pain management: therapeutic potential and mechanisms of action of the new high-concentration capsaicin 8% patch. Br J Anaesth 2011;107:490–502. https://doi.org/10.1093/bja/aer260.
10.1093/bja/aer260 ↗57. Babbar, S, Marier, JF, Mouksassi, MS, Beliveau, M, Vanhove, GF, Chanda, S, et al.. Pharmacokinetic analysis of capsaicin after topical administration of a high-concentration capsaicin patch to patients with peripheral neuropathic pain. Ther Drug Monit 2009;31:502–10. https://doi.org/10.1097/ftd.0b013e3181a8b200.
10.1097/FTD.0b013e3181a8b200 ↗58. Craciunescu, O, Icriverzi, M, Florian, PE, Roseanu, A, Trif, M. Mechanisms and pharmaceutical action of lipid nanoformulation of natural bioactive compounds as efficient delivery systems in the therapy of osteoarthritis. Pharmaceutics 2021;13:1108. https://doi.org/10.3390/pharmaceutics13081108.
10.3390/pharmaceutics13081108 ↗59. Wen, J, Li, H, Dai, H, Hua, S, Long, X, Li, H, et al.. Intra-articular nanoparticles based therapies for osteoarthritis and rheumatoid arthritis management. Mater Today Bio 2023;19:100597. https://doi.org/10.1016/j.mtbio.2023.100597.
10.1016/j.mtbio.2023.100597 ↗60. Huang, K, Li, Q, Lin, H, Shen, Q, Wu, Y, Tian, T, et al.. Cartilage‐penetrating framework nucleic acid nanoparticles ameliorate osteoarthritis by promoting drug delivery and chondrocyte uptake. Adv Sci 2025;12:2502661. https://doi.org/10.1002/advs.202502661.
10.1002/advs.202502661 ↗61. Morici, L, Allémann, E, Rodríguez-Nogales, C, Jordan, O. Cartilage-targeted drug nanocarriers for osteoarthritis therapy. Int J Pharm 2024;666:124843. https://doi.org/10.1016/j.ijpharm.2024.124843.
10.1016/j.ijpharm.2024.124843 ↗62. Shi, T, Zhao, J, Long, K, Gao, M, Chen, F, Chen, X, et al.. Cationic mesoporous silica nanoparticles alleviate osteoarthritis by targeting multiple inflammatory mediators. Biomaterials 2023;303:122366. https://doi.org/10.1016/j.biomaterials.2023.122366.
10.1016/j.biomaterials.2023.122366 ↗63. Xu, YD, Liang, XC, Li, ZP, Wu, ZS, Yang, J, Jia, SZ, et al.. Apoptotic body-inspired nanotherapeutics efficiently attenuate osteoarthritis by targeting BRD4-regulated synovial macrophage polarization. Biomaterials 2024;306:122483. https://doi.org/10.1016/j.biomaterials.2024.122483.
10.1016/j.biomaterials.2024.122483 ↗64. Wang, D, Pan, Y, Chen, W, He, D, Qi, W, Chen, J, et al.. Nanodrugs targeting key factors of ferroptosis regulation for enhanced treatment of osteoarthritis. Adv Sci 2025;12:2412817. https://doi.org/10.1002/advs.202412817.
10.1002/advs.202412817 ↗65. Zhan, M, Sun, H, Wang, Z, Li, G, Yang, R, Mignani, S, et al.. Nanoparticle-mediated multiple modulation of bone microenvironment to tackle osteoarthritis. ACS Nano 2024;18:10625–41. https://doi.org/10.1021/acsnano.4c00909.
10.1021/acsnano.4c00909 ↗66. Sheng, W, Li, A, Yue, Y, Wang, Q, Yu, F, Weng, J, et al.. A novel curcumin‐loaded nanoplatform alleviates osteoarthritis by inhibiting chondrocyte ferroptosis. Macromol Rapid Commun 2025;46:2400495. https://doi.org/10.1002/marc.202400495.
10.1002/marc.202400495 ↗67. Xue, X, Liu, H, Wang, S, Hu, Y, Huang, B, Li, M, et al.. Neutrophil-erythrocyte hybrid membrane-coated hollow copper sulfide nanoparticles for targeted and photothermal/anti-inflammatory therapy of osteoarthritis. Compos B Eng 2022;237:109855. https://doi.org/10.1016/j.compositesb.2022.109855.
10.1016/j.compositesb.2022.109855 ↗68. Xue, S, Ruan, G, Li, J, Madry, H, Zhang, C, Ding, C. Bio-responsive and multi-modality imaging nanomedicine for osteoarthritis theranostics. Biomater Sci 2023;11:5095–107. https://doi.org/10.1039/d3bm00370a.
10.1039/D3BM00370A ↗69. Xue, C, Tian, J, Cui, Z, Liu, Y, Sun, D, Xiong, M, et al.. Reactive oxygen species (ROS)-mediated M1 macrophage-dependent nanomedicine remodels inflammatory microenvironment for osteoarthritis recession. Bioact Mater 2024;33:545–61. https://doi.org/10.1016/j.bioactmat.2023.10.032.
10.1016/j.bioactmat.2023.10.032 ↗70. Lu, H, Wei, J, Liu, K, Li, Z, Xu, T, Yang, D, et al.. Radical-scavenging and subchondral bone-regenerating nanomedicine for osteoarthritis treatment. ACS Nano 2023;17:6131–46. https://doi.org/10.1021/acsnano.3c01789.
10.1021/acsnano.3c01789 ↗71. Lu, F, Wu, SH, Hung, Y, Mou, CY. Size effect on cell uptake in well-suspended, uniform mesoporous silica nanoparticles. Small 2009;5:1408–13. https://doi.org/10.1002/smll.200900005.
10.1002/smll.200900005 ↗72. Trewyn, BG, Nieweg, JA, Zhao, Y, Lin, VS. Biocompatible mesoporous silica nanoparticles with different morphologies for animal cell membrane penetration. Chem Eng J 2008;137:23–9. https://doi.org/10.1016/j.cej.2007.09.045.
10.1016/j.cej.2007.09.045 ↗73. Moghimi, SM, Hunter, AC, Murray, JC. Long-circulating and target-specific nanoparticles: theory to practice. Pharmacol Rev 2001;53:283–318. https://doi.org/10.1016/s0031-6997(24)01494-7.
10.1016/S0031-6997(24)01494-7 ↗74. Panyam, J, Dali, MM, Sahoo, SK, Ma, W, Chakravarthi, SS, Amidon, GL, et al.. Polymer degradation and in vitro release of a model protein from poly (D, L-lactide-co-glycolide) nano-and microparticles. J Contr Release 2003;92:173–87. https://doi.org/10.1016/s0168-3659(03)00328-6.
10.1016/S0168-3659(03)00328-6 ↗75. Jeong, JH, Kim, SW, Park, TG. Molecular design of functional polymers for gene therapy. Prog Polym Sci 2007;32:1239–74. https://doi.org/10.1016/j.progpolymsci.2007.05.019.
10.1016/j.progpolymsci.2007.05.019 ↗76. Samad, A, Sultana, Y, Aqil, M. Liposomal drug delivery systems: an update review. Curr Drug Deliv 2007;4:297–305. https://doi.org/10.2174/156720107782151269.
10.2174/156720107782151269 ↗77. Liu, Z, Li, X, Xiu, B, Duan, C, Li, J, Zhang, X, et al.. A novel and simple preparative method for uniform-sized PLGA microspheres: preliminary application in antitubercular drug delivery. Colloids Surf B Biointerfaces 2016;145:679–87. https://doi.org/10.1016/j.colsurfb.2016.05.085.
10.1016/j.colsurfb.2016.05.085 ↗78. Tabata, Y, Ikada, Y. Phagocytosis of polymer microspheres by macrophages. New Polym Mater 2005;10:107–41.
10.1007/BFb0043062 ↗79. Geng, YA, Dalhaimer, P, Cai, S, Tsai, R, Tewari, M, Minko, T, et al.. Shape effects of filaments versus spherical particles in flow and drug delivery. Nat Nanotechnol 2007;2:249–55. https://doi.org/10.1038/nnano.2007.70.
10.1038/nnano.2007.70 ↗80. Nishiyama, N. Nanomedicine: nanocarriers shape up for long life. Nat Nanotechnol 2007;2:203–4. https://doi.org/10.1038/nnano.2007.88.
10.1038/nnano.2007.88 ↗81. Hodes, G. When small is different: some recent advances in concepts and applications of nanoscale phenomena. Adv Mater 2007;19:639–55. https://doi.org/10.1002/adma.200790035.
10.1002/adma.200601173 ↗82. Auffan, M, Rose, J, Bottero, JY, Lowry, GV, Jolivet, JP, Wiesner, MR. Towards a definition of inorganic nanoparticles from an environmental, health and safety perspective. Nat Nanotechnol 2009;4:634–41. https://doi.org/10.1038/nnano.2009.242.
10.1038/nnano.2009.242 ↗83. Sharma, D, Sharma, N, Pathak, M, Agrawala, PK, Basu, M, Ojha, H. Nanotechnology-based drug delivery systems: challenges and opportunities. Drug Target Stimuli Sensitive Drug Deliv Syst 2018;1:39–79.
10.1016/B978-0-12-813689-8.00002-1 ↗84. Prakash, S, Kulamarva, AG. Recent advances in drug delivery: potential and limitations of carbon nanotubes. Recent Pat Drug Deliv Formul 2007;1:214–2. https://doi.org/10.2174/187221107782331601.
10.2174/187221107782331601 ↗85. Salata, OV. Applications of nanoparticles in biology and medicine. J Nanobiotechnol 2004;2:1–6. https://doi.org/10.1186/1477-3155-2-3.
10.1186/1477-3155-2-3 ↗86. Ravichandran, R. Nanotechnology-based drug delivery systems. NanoBiotechnology 2009;5:17–33. https://doi.org/10.1007/s12030-009-9028-2.
10.1007/s12030-009-9028-2 ↗87. Keck, CM, Müller, RH. Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation. Eur J Pharm Biopharm 2006;62:3–16. https://doi.org/10.1016/j.ejpb.2005.05.009.
10.1016/j.ejpb.2005.05.009 ↗88. Thassu, D, Pathak, Y, Deleers, M. Nanoparticulate drug delivery systems. an overview. In: Thassu D, Deleers M, Pathak Y, editors. Nanoparticulate drug delivery systems. New York: Informa Healthcare; 2007:1–31 pp.”
10.1201/9781420008449-1 ↗89. Shinde, AJ, Tyagi, R. Solubilization of poorly soluble drugs: a review. Pharmainfo. net 2007;5:36–44.
90. Chaubal, MV. Application of formulation technologies in lead candidate selection and optimization. Drug Discov Today 2004;9:603–9. https://doi.org/10.1016/s1359-6446(04)03171-x.
10.1016/S1359-6446(04)03171-X ↗91. Basa, S, Muniyappan, T, Karatgi, P, Prabhu, R, Pillai, R. Production and in vitro characterization of solid dosage form incorporating drug nanoparticles. Drug Dev Ind Pharm 2008;34:1209–18. https://doi.org/10.1080/03639040802005024.
10.1080/03639040802005024 ↗92. Muller, RH. Nanosuspension for the formulation of poorly soluble drugs. In: Neilloud, F and Marti-Mestres, G, editors, pharmaceutical emulsion and suspension.
93. Mozafari, M. Nanotechnology in wound care: one step closer to the clinic. Mol Ther 2018;26:2085–6. https://doi.org/10.1016/j.ymthe.2018.08.008.
10.1016/j.ymthe.2018.08.008 ↗94. Bobo, D, Robinson, KJ, Islam, J, Thurecht, KJ, Corrie, SR. Nanoparticle-based medicines: a review of FDA-approved materials and clinical trials to date. Pharm Res 2016;33:2373–87. https://doi.org/10.1007/s11095-016-1958-5.
10.1007/s11095-016-1958-5 ↗95. Sahu, T, Ratre, YK, Chauhan, S, Bhaskar, LV, Nair, MP, Verma, HK. Nanotechnology based drug delivery system: current strategies and emerging therapeutic potential for medical science. J Drug Deliv Sci Technol 2021;63:102487. https://doi.org/10.1016/j.jddst.2021.102487.
10.1016/j.jddst.2021.102487 ↗96. Bajracharya, R, Song, JG, Back, SY, Han, HK. Recent advancements in non-invasive formulations for protein drug delivery. Comput Struct Biotechnol J 2019;17:1290–308. https://doi.org/10.1016/j.csbj.2019.09.004.
10.1016/j.csbj.2019.09.004 ↗97. Laura, IM, Dosio, F, Cattel, L. Stealth liposomes: review of the basic science, rationale, and clinical applications, existing and potential. Int J nanomedicine 2006;1:297–315.
98. Akbarzadeh, A, Rezaei-Sadabady, R, Davaran, S, Joo, SW, Zarghami, N, Hanifehpour, Y, et al.. Liposome: classification, preparation, and applications. Nanoscale Res Lett 2013;8:1–9. https://doi.org/10.1186/1556-276x-8-102.
10.1186/1556-276X-8-102 ↗99. Kedar, U, Phutane, P, Shidhaye, S, Kadam, V. Advances in polymeric micelles for drug delivery and tumor targeting. Nanomed Nanotechnol Biol Med 2010;6:714–29. https://doi.org/10.1016/j.nano.2010.05.005.
10.1016/j.nano.2010.05.005 ↗100. Kahraman, E, Güngör, S, Özsoy, Y. Potential enhancement and targeting strategies of polymeric and lipid-based nanocarriers in dermal drug delivery. Ther Deliv 2017;8:967–85. https://doi.org/10.4155/tde-2017-0075.
10.4155/tde-2017-0075 ↗