An updated review on the modifications, recycling, polymerization, and applications of polymethyl methacrylate (PMMA)
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OpenAlex topics: Advanced Polymer Synthesis and Characterization · Photopolymerization techniques and applications · biodegradable polymer synthesis and properties
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References (100+)
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1. Alqutaibi AY, Baik A, Almuzaini SA et al (2023) Polymeric denture base materials: a review. Polymers (Basel) 15:3258. https://doi.org/10.3390/polym1515325810.3390/polym15153258 ↗
2. Mostafavi AH, Mishra AK, Gallucci F et al (2023) Advances in surface modification and functionalization for tailoring the characteristics of thin films and membranes via chemical vapor deposition techniques. J Appl Polym Sci. https://doi.org/10.1002/app.5372010.1002/app.53720 ↗
3. Purohit P, Bhatt A, Mittal RK et al (2023) Polymer grafting and its chemical reactions. Front Bioeng Biotechnol. https://doi.org/10.3389/fbioe.2022.104492710.3389/fbioe.2022.1044927 ↗
4. Sansul S, Yousif E, Ahmed DS et al (2023) Pendant modification of poly(methyl methacrylate) to enhance Its stability against photoirradiation. Polymers (Basel) 15:2989. https://doi.org/10.3390/polym1514298910.3390/polym15142989 ↗
5. Tardy BL, Mattos BD, Otoni CG et al (2021) Deconstruction and reassembly of renewable polymers and biocolloids into next generation structured materials. Chem Rev 121:14088–14188. https://doi.org/10.1021/acs.chemrev.0c0133310.1021/acs.chemrev.0c01333 ↗
6. Zafar MS (2020) Prosthodontic applications of polymethyl methacrylate (PMMA): an update. Polymers (Basel) 12:2299. https://doi.org/10.3390/polym1210229910.3390/polym12102299 ↗
7. Forte MA, Silva RM, Tavares CJ, Silva RF (2021) Is poly(methyl methacrylate) (PMMA) a suitable substrate for ALD?: a review. Polymers (Basel) 13:1346. https://doi.org/10.3390/polym1308134610.3390/polym13081346 ↗
8. Ibraheem HA, El-Hiti GA, Yousif E et al (2024) Investigation of the impact of chemical modifications on the photostability of polymethyl methacrylate. Int J Polym Sci 2024:1–14. https://doi.org/10.1155/2024/335428010.1155/2024/3354280 ↗
9. Karimi S, Helal E, Gutierrez G et al (2020) A review on graphene’s light stabilizing effects for reduced photodegradation of polymers. Crystals 11:3. https://doi.org/10.3390/cryst1101000310.3390/cryst11010003 ↗
10. Andrady AL, Heikkilä AM, Pandey KK et al (2023) Effects of UV radiation on natural and synthetic materials. Photochem Photobiol Sci 22:1177–1202. https://doi.org/10.1007/s43630-023-00377-610.1007/s43630-023-00377-6 ↗
11. Yousif E, El-Hiti G, Haddad R, Balakit A (2015) Photochemical stability and photostabilizing efficiency of poly(methyl methacrylate) based on 2-(6-methoxynaphthalen-2-yl)propanoate metal ion complexes. Polymers (Basel) 7:1005–1019. https://doi.org/10.3390/polym706100510.3390/polym7061005 ↗
12. Yang S, Karve VV, Justin A et al (2021) Enhancing MOF performance through the introduction of polymer guests. Coord Chem Rev 427:213525. https://doi.org/10.1016/j.ccr.2020.21352510.1016/j.ccr.2020.213525 ↗
13. Yousefi F, Mousavi SB, Heris SZ, Naghash-Hamed S (2023) UV-shielding properties of a cost-effective hybrid PMMA-based thin film coatings using TiO2 and ZnO nanoparticles: a comprehensive evaluation. Sci Rep 13:7116. https://doi.org/10.1038/s41598-023-34120-z10.1038/s41598-023-34120-z ↗
14. Raczuk E, Dmochowska B, Samaszko-Fiertek J, Madaj J (2022) Different Schiff bases—structure, importance and classification. Molecules 27:787. https://doi.org/10.3390/molecules2703078710.3390/molecules27030787 ↗
15. Dimassi SN, Hahladakis JN, Yahia MND et al (2022) Degradation-fragmentation of marine plastic waste and their environmental implications: a critical review. Arab J Chem 15:104262. https://doi.org/10.1016/j.arabjc.2022.10426210.1016/j.arabjc.2022.104262 ↗
16. Kristoffersen KA, van Amerongen A, Böcker U et al (2020) Fourier-transform infrared spectroscopy for monitoring proteolytic reactions using dry-films treated with trifluoroacetic acid. Sci Rep 10:7844. https://doi.org/10.1038/s41598-020-64583-310.1038/s41598-020-64583-3 ↗
17. Everts PA, Lana JF, Onishi K et al (2023) Angiogenesis and tissue repair depend on platelet dosing and bioformulation strategies following orthobiological platelet-rich plasma procedures: a narrative review. Biomedicines 11:1922. https://doi.org/10.3390/biomedicines1107192210.3390/biomedicines11071922 ↗
18. Kim K, Lee J-W, Park B-G et al (2022) Investigation of correlative parameters to evaluate EUV lithographic performance of PMMA. RSC Adv 12:2589–2594. https://doi.org/10.1039/D1RA07291A10.1039/D1RA07291A ↗
19. El-Hiti GA, Ahmed DS, Yousif E et al (2021) Modifications of polymers through the addition of ultraviolet absorbers to reduce the aging effect of accelerated and natural irradiation. Polymers (Basel) 14:20. https://doi.org/10.3390/polym1401002010.3390/polym14010020 ↗
20. Trujillo Villanueva LE, Legorreta García F, Pérez Moreno F et al (2021) Ultraviolet light effects on cobalt-thiourea complexes crystallization. Crystals 11:473. https://doi.org/10.3390/cryst1105047310.3390/cryst11050473 ↗
21. Moens E, De Smit K, Marien Y et al (2020) Progress in reaction mechanisms and reactor technologies for thermochemical recycling of poly(methyl methacrylate). Polymers (Basel) 12:1667. https://doi.org/10.3390/polym1208166710.3390/polym12081667 ↗
22. Ashfaq A, Clochard M-C, Coqueret X et al (2020) Polymerization reactions and modifications of polymers by ionizing radiation. Polymers (Basel) 12:2877. https://doi.org/10.3390/polym1212287710.3390/polym12122877 ↗
23. Przesławski G, Szcześniak K, Gajewski P, Marcinkowska A (2022) Influence of initiator concentration on the polymerization course of methacrylate bone cement. Polymers (Basel) 14:5005. https://doi.org/10.3390/polym1422500510.3390/polym14225005 ↗
24. Yan W, de la Vega J, Eroğlu Ö et al (2024) High power sunlight-simulated UV-induced radical polymerization: self-initiation and self-crosslinking. Macromol Mater Eng. https://doi.org/10.1002/mame.20230045610.1002/mame.202300456 ↗
25. Jennings SJA, Hambrey MJ (2021) Structures and deformation in glaciers and ice sheets. Rev Geophys. https://doi.org/10.1029/2021RG00074310.1029/2021RG000743 ↗
26. Heuts JPA, Russell GT (2006) The nature of the chain-length dependence of the propagation rate coefficient and its effect on the kinetics of free-radical polymerization. 1. Small-mol stud Eur Polym J 42:3–20. https://doi.org/10.1016/j.eurpolymj.2005.09.02210.1016/j.eurpolymj.2005.09.022 ↗
27. Eills J, Budker D, Cavagnero S et al (2023) Spin hyperpolarization in modern magnetic resonance. Chem Rev 123:1417–1551. https://doi.org/10.1021/acs.chemrev.2c0053410.1021/acs.chemrev.2c00534 ↗
28. Pirman T, Ocepek M, Likozar B (2021) Radical polymerization of acrylates, methacrylates, and styrene: biobased approaches, mechanism, kinetics, secondary reactions, and modeling. Ind Eng Chem Res 60:9347–9367. https://doi.org/10.1021/acs.iecr.1c0164910.1021/acs.iecr.1c01649 ↗
29. Ribeiro HJS, Ferreira AC, Ferreira CC et al (2024) Depolymerization of PMMA-based dental resin scraps on different production scales. Energies 17:1196. https://doi.org/10.3390/en1705119610.3390/en17051196 ↗
30. Ohno T, Tashiro S, Amano Y et al (2021) Consistent modelling of material weight loss and gas release due to pyrolysis and conducting benchmark tests of the model—a case for glovebox panel materials such as polymethyl methacrylate. PLoS ONE 16:e0245303. https://doi.org/10.1371/journal.pone.024530310.1371/journal.pone.0245303 ↗
31. Qiu Z, Neumann CN (2024) Influence of cage effects in directing the outcome of C-X bond forming reactions. ACS Org Inorg Au 4:1–25. https://doi.org/10.1021/acsorginorgau.3c0004410.1021/acsorginorgau.3c00044 ↗
32. Moens EKC, Marien YW, Trigilio AD et al (2023) Kinetic monte carlo convergence demands for thermochemical recycling kinetics of vinyl polymers with dominant depropagation. Processes 11:1623. https://doi.org/10.3390/pr1106162310.3390/pr11061623 ↗
33. Ballard N, Veloso A, Asua JM (2018) Mid-chain radical migration in the radical polymerization of n-butyl acrylate. Polymers (Basel) 10:765. https://doi.org/10.3390/polym1007076510.3390/polym10070765 ↗
34. Stoliarov SI, Westmoreland PR, Nyden MR, Forney GP (2003) A reactive molecular dynamics model of thermal decomposition in polymers: I. poly(methyl methacrylate). Polymer (Guildf) 44:883–894. https://doi.org/10.1016/S0032-3861(02)00761-910.1016/S0032-3861(02)00761-9 ↗
35. Mancuso G, Midiri A, Gerace E, Biondo C (2021) Bacterial antibiotic resistance: the most critical pathogens. Pathogens 10:1310. https://doi.org/10.3390/pathogens1010131010.3390/pathogens10101310 ↗
36. Kehribar L, Aydın M, Coşkun HS, Surucu S (2023) Silver nanoparticles enhance the antibacterial effect of antibiotic-loaded bone cement. Cureus. https://doi.org/10.7759/cureus.3499210.7759/cureus.34992 ↗
37. Gupta A, Mumtaz S, Li C-H et al (2019) Combatting antibiotic-resistant bacteria using nanomaterials. Chem Soc Rev 48:415–427. https://doi.org/10.1039/C7CS00748E10.1039/C7CS00748E ↗
38. Sim S, Wong N (2021) Nanotechnology and its use in imaging and drug delivery (Review). Biomed Rep 14:42. https://doi.org/10.3892/br.2021.141810.3892/br.2021.1418 ↗
39. Choi YS, Kim YH, An HM et al (2023) Efficacy of silver nanoparticles-loaded bone cement against an MRSA induced-osteomyelitis in a rat model. Medicina (B Aires) 59:811. https://doi.org/10.3390/medicina5904081110.3390/medicina59040811 ↗
40. Liao C, Li Y, Tjong SC (2018) Graphene nanomaterials: synthesis, biocompatibility, and cytotoxicity. Int J Mol Sci 19:3564. https://doi.org/10.3390/ijms1911356410.3390/ijms19113564 ↗
41. Patel V, Joshi U, Joshi A et al (2023) Cytotoxicity analysis for the hydroxyl functionalized MWCNT reinforced PMMA nanocomposites in oral squamous carcinoma (KB) cells. Polymers (Basel) 15:1192. https://doi.org/10.3390/polym1505119210.3390/polym15051192 ↗
42. Luo T, Ma Y, Cui X (2024) Review on frontal polymerization behavior for thermosetting resins: materials. Model Appl Polym (Basel) 16:185. https://doi.org/10.3390/polym1602018510.3390/polym16020185 ↗
43. Liu X, Cheng C, Peng X et al (2019) A promising material for bone repair: PMMA bone cement modified by dopamine-coated strontium-doped calcium polyphosphate particles. R Soc Open Sci 6:191028. https://doi.org/10.1098/rsos.19102810.1098/rsos.191028 ↗
44. Quan Q, Gongping X, Ruisi N, Shiwen L (2023) New research progress of modified bone cement applied to vertebroplasty. World Neurosurg 176:10–18. https://doi.org/10.1016/j.wneu.2023.04.04810.1016/j.wneu.2023.04.048 ↗
45. Zhu X, Wang C, Bai H et al (2023) Functionalization of biomimetic mineralized collagen for bone tissue engineering. Mater Today Bio 20:100660. https://doi.org/10.1016/j.mtbio.2023.10066010.1016/j.mtbio.2023.100660 ↗
46. Zhu J, Yang S, Cai K et al (2020) Bioactive poly (methyl methacrylate) bone cement for the treatment of osteoporotic vertebral compression fractures. Theranostics 10:6544–6560. https://doi.org/10.7150/thno.4442810.7150/thno.44428 ↗
47. Li S, Li X, Bai X et al (2024) A meta-analysis comparing the efficacy of mineralized collagen-polymethylmethacrylate and polymethylmethacrylate bone cements in the treatment of vertebral compression fractures. PLoS ONE 19:e0299325. https://doi.org/10.1371/journal.pone.029932510.1371/journal.pone.0299325 ↗
48. Shirdar MR, Taheri MM, Qi M-L et al (2021) Optimization of the mechanical properties and the cytocompatibility for the pmma nanocomposites reinforced with the hydroxyapatite nanofibers and the magnesium phosphate nanosheets. Materials (Basel) 14:5893. https://doi.org/10.3390/ma1419589310.3390/ma14195893 ↗
49. Yuan M, Huang D, Zhao Y (2022) Development of synthesis and application of high molecular weight poly(methyl methacrylate). Polymers (Basel) 14:2632. https://doi.org/10.3390/polym1413263210.3390/polym14132632 ↗
50. Simič R, Mandal J, Zhang K, Spencer ND (2021) Oxygen inhibition of free-radical polymerization is the dominant mechanism behind the “mold effect” on hydrogels. Soft Matter 17:6394–6403. https://doi.org/10.1039/D1SM00395J10.1039/D1SM00395J ↗
51. Shiho H, DeSimone JM (2001) Dispersion polymerization of glycidyl methacrylate in supercritical carbon dioxide. Macromolecules 34:1198–1203. https://doi.org/10.1021/ma001007410.1021/ma0010074 ↗
52. Lepilleur C, Beckman EJ (1997) Dispersion polymerization of methyl methacrylate in supercritical CO 2. Macromolecules 30:745–756. https://doi.org/10.1021/ma960764s10.1021/ma960764s ↗
53. Wang Z, Yang YJ, Dong QZ, Hu CP (2008) Free radical polymerizations of some vinyl monomers in carbon dioxide fluid. J Appl Polym Sci 110:468–474. https://doi.org/10.1002/app.2853210.1002/app.28532 ↗
54. Sharma S, Verma A, Rangappa SM et al (2023) Recent progressive developments in conductive-fillers based polymer nanocomposites (CFPNC’s) and conducting polymeric nanocomposites (CPNC’s) for multifaceted sensing applications. J Mater Res Technol 26:5921–5974. https://doi.org/10.1016/j.jmrt.2023.08.30010.1016/j.jmrt.2023.08.300 ↗
55. Zhang S, Dang Y, Ni X et al (2021) Preparation and stabilization of high molecular weight poly(acrylonitrile-co-2-methylenesuccinamic acid) for carbon fiber precursor. Polymers (Basel) 13:3862. https://doi.org/10.3390/polym1322386210.3390/polym13223862 ↗
56. Yeum J-H, Deng Y (2005) Synthesis of high molecular weight poly(methyl methacrylate) microspheres by suspension polymerization in the presence of silver nanoparticles. Colloid Polym Sci 283:1172–1179. https://doi.org/10.1007/s00396-005-1300-y10.1007/s00396-005-1300-y ↗
57. Pulingam T, Foroozandeh P, Chuah J-A, Sudesh K (2022) Exploring various techniques for the chemical and biological synthesis of polymeric nanoparticles. Nanomaterials 12:576. https://doi.org/10.3390/nano1203057610.3390/nano12030576 ↗
58. Zhang P, Xu Q, Mao W et al (2023) Synthesis of ultrahigh molecular weight poly(methyl methacrylate) via the polymerization of MMA initiated by the combination of palladium carboxylates with thiols. Polymers (Basel) 15:2501. https://doi.org/10.3390/polym1511250110.3390/polym15112501 ↗
59. Nyabadza A, McCarthy É, Makhesana M et al (2023) A review of physical, chemical and biological synthesis methods of bimetallic nanoparticles and applications in sensing, water treatment, biomedicine, catalysis and hydrogen storage. Adv Colloid Interface Sci 321:103010. https://doi.org/10.1016/j.cis.2023.10301010.1016/j.cis.2023.103010 ↗
60. Zhu Y, Egap E (2021) Light-mediated polymerization induced by semiconducting nanomaterials: state-of-the-art and future perspectives. ACS Polym Au 1:76–99. https://doi.org/10.1021/acspolymersau.1c0001410.1021/acspolymersau.1c00014 ↗
61. Coban ZG, Kiliclar HC, Yagci Y (2023) Photoinitiated cationic ring-opening polymerization of octamethylcyclotetrasiloxane. Molecules 28:1299. https://doi.org/10.3390/molecules2803129910.3390/molecules28031299 ↗
62. Yang H, Du J (2023) Crystallinity, rheology, and mechanical properties of low-/high-molecular-weight PLA blended systems. Molecules 29:169. https://doi.org/10.3390/molecules2901016910.3390/molecules29010169 ↗
63. Lutz J, Börner HG, Weichenhan K (2005) Combining atom transfer radical polymerization and click chemistry: a versatile method for the preparation of end-functional polymers. Macromol Rapid Commun 26:514–518. https://doi.org/10.1002/marc.20050000210.1002/marc.200500002 ↗
64. Tang W, Tsarevsky NV, Matyjaszewski K (2006) Determination of equilibrium constants for atom transfer radical polymerization. J Am Chem Soc 128:1598–1604. https://doi.org/10.1021/ja055859110.1021/ja0558591 ↗
65. Xue L, Agarwal US, Lemstra PJ (2002) High molecular weight PMMA by ATRP. Macromolecules 35:8650–8652. https://doi.org/10.1021/ma020905s10.1021/ma020905s ↗
66. Dworakowska S, Lorandi F, Gorczyński A, Matyjaszewski K (2022) Toward green atom transfer radical polymerization: current status and future challenges. Adv Sci. https://doi.org/10.1002/advs.20210607610.1002/advs.202106076 ↗
67. Zaborniak I, Klamut M, Warne CM et al (2024) Controlled polymer synthesis toward green chemistry: deep insights into atom transfer radical polymerization in biobased substitutes for polar aprotic solvents. ACS Sustain Chem Eng 12:4933–4945. https://doi.org/10.1021/acssuschemeng.3c0799310.1021/acssuschemeng.3c07993 ↗
68. Jeon HJ, Youk JH, Ahn SH et al (2009) Synthesis of high molecular weight 3-arm star PMMA by ARGET ATRP. Macromol Res 17:240–244. https://doi.org/10.1007/BF0321868610.1007/BF03218686 ↗
69. Arita T, Kayama Y, Ohno K et al (2008) High-pressure atom transfer radical polymerization of methyl methacrylate for well-defined ultrahigh molecular-weight polymers. Polymer (Guildf) 49:2426–2429. https://doi.org/10.1016/j.polymer.2008.03.02610.1016/j.polymer.2008.03.026 ↗
70. Song Z, Wang S, Gao R et al (2023) Recent advancements in mechanistic studies of palladium- and nickel-catalyzed ethylene copolymerization with polar monomers. Polymers (Basel) 15:4343. https://doi.org/10.3390/polym1522434310.3390/polym15224343 ↗
71. More MS, Joshi PG, Mishra YK, Khanna PK (2019) Metal complexes driven from Schiff bases and semicarbazones for biomedical and allied applications: a review. Mater Today Chem 14:100195. https://doi.org/10.1016/j.mtchem.2019.10019510.1016/j.mtchem.2019.100195 ↗
72. Lee J, Yoon M, Lee H, Nayab S (2020) Stereoselective polymerization of methyl methacrylate and rac-lactide mediated by iminomethylpyridine based Cu(ii) complexes. RSC Adv 10:16209–16220. https://doi.org/10.1039/D0RA00805B10.1039/D0RA00805B ↗
73. Nguyen MN, Margaillan A, Pham QT, Bressy C (2018) RAFT Polymerization of tert-butyldimethylsilyl methacrylate: kinetic study and determination of rate coefficients. Polymers (Basel) 10:224. https://doi.org/10.3390/polym1002022410.3390/polym10020224 ↗
74. Yuan M, Huang D, Wang Z et al (2022) Synthesis of ultra-high molecular weight poly(methyl methacrylate) with hydrosilane as initiator. Mater Today Commun 33:104927. https://doi.org/10.1016/j.mtcomm.2022.10492710.1016/j.mtcomm.2022.104927 ↗
75. Rui J, Cheng S, Ren H et al (2024) Electric field effect of the plasma-initiated polymerization of methyl methacrylate: a negatively charged long-lived radical. Polymers (Basel) 16:1497. https://doi.org/10.3390/polym1611149710.3390/polym16111497 ↗
76. Ahamad Said MN, Hasbullah NA, Rosdi MRH et al (2022) Polymerization and applications of poly(methyl methacrylate)–graphene oxide nanocomposites: a review. ACS Omega 7:47490–47503. https://doi.org/10.1021/acsomega.2c0448310.1021/acsomega.2c04483 ↗
77. Chen J, Garcia ES, Zimmerman SC (2020) Intramolecularly cross-linked polymers: from structure to function with applications as artificial antibodies and artificial enzymes. Acc Chem Res 53:1244–1256. https://doi.org/10.1021/acs.accounts.0c0017810.1021/acs.accounts.0c00178 ↗
78. Ceylan G, Emik S, Yalcinyuva T et al (2023) The effects of cross-linking agents on the mechanical properties of poly (methyl methacrylate) resin. Polymers (Basel) 15:2387. https://doi.org/10.3390/polym1510238710.3390/polym15102387 ↗
79. Hussein MA (2017) Role of cross-linking process on the performance of PMMA. Int J Biosens Bioelectron. https://doi.org/10.15406/ijbsbe.2017.03.0006510.15406/ijbsbe.2017.03.00065 ↗
80. Grillo A, Rusconi Y, D’Alterio MC et al (2024) Ring opening polymerization of six- and eight-membered racemic cyclic esters for biodegradable materials. Int J Mol Sci 25:1647. https://doi.org/10.3390/ijms2503164710.3390/ijms25031647 ↗
81. Wurm F, Rietzler B, Pham T, Bechtold T (2020) Multivalent Ions as reactive crosslinkers for biopolymers—a review. Molecules 25:1840. https://doi.org/10.3390/molecules2508184010.3390/molecules25081840 ↗
82. Naikwadi AT, Sharma BK, Bhatt KD, Mahanwar PA (2022) Gamma radiation processed polymeric materials for high performance applications: a review. Front Chem. https://doi.org/10.3389/fchem.2022.83711110.3389/fchem.2022.837111 ↗
83. Aldayel AA, Alwael HM, Alshathri RM et al (2022) A comparison between cross-linking protocols in patients with progressive keratoconus: a review. Cureus. https://doi.org/10.7759/cureus.3102910.7759/cureus.31029 ↗
84. Kechagias JD, Zaoutsos SP, Fountas NA, Vaxevanidis NM (2024) Experimental investigation and neural network development for modeling tensile properties of polymethyl methacrylate (PMMA) filament material. Int J Adv Manuf Technol 134:4387–4398. https://doi.org/10.1007/s00170-024-14402-010.1007/s00170-024-14402-0 ↗
85. Li X, Li L, Zheng Y et al (2023) A study of the compressive behavior of recycled rubber concrete reinforced with hybrid fibers. Materials (Basel) 16:4731. https://doi.org/10.3390/ma1613473110.3390/ma16134731 ↗
86. Yerliyurt K, Taşdelen TB, Eğri Ö, Eğri S (2023) Flexural properties of heat-polymerized PMMA denture base resins reinforced with fibers with different characteristics. Polymers (Basel) 15:3211. https://doi.org/10.3390/polym1515321110.3390/polym15153211 ↗
87. Hung J-P, Bai Y-W, Hung C-Q, Lee T-E (2019) Biomechanical performance of the cemented hip stem with different surface finish. Appl Sci 9:4082. https://doi.org/10.3390/app919408210.3390/app9194082 ↗
88. von Hertzberg-Boelch SP, Luedemann M, Rudert M, Steinert AF (2022) PMMA bone cement: antibiotic elution and mechanical properties in the context of clinical use. Biomedicines 10:1830. https://doi.org/10.3390/biomedicines1008183010.3390/biomedicines10081830 ↗
89. Hernigou P, Daltro G, Lachaniette CHF et al (2009) Fixation of the cemented stem: clinical relevance of the porosity and thickness of the cement mantle. Open Orthop J 3:8–13. https://doi.org/10.2174/187432500090301000810.2174/1874325000903010008 ↗
90. Pujari-Palmer M, Robo C, Persson C et al (2018) Influence of cement compressive strength and porosity on augmentation performance in a model of orthopedic screw pull-out. J Mech Behav Biomed Mater 77:624–633. https://doi.org/10.1016/j.jmbbm.2017.10.01610.1016/j.jmbbm.2017.10.016 ↗
91. Hamdy TM (2024) Modification of polymethylmethacrylate bone cement with halloysite clay nanotubes. BMC Oral Health 24:893. https://doi.org/10.1186/s12903-024-04600-310.1186/s12903-024-04600-3 ↗
92. Arora M (2013) Polymethylmethacrylate bone cements and additives: A review of the literature. World J Orthop 4:67. https://doi.org/10.5312/wjo.v4.i2.6710.5312/wjo.v4.i2.67 ↗
93. Zhang Y, Xiao J, Yang H et al (2019) N-acetyl cysteine as a novel polymethyl methacrylate resin component: protection against cell apoptosis and genotoxicity. Oxid Med Cell Longev 2019:1–12. https://doi.org/10.1155/2019/130173610.1155/2019/1301736 ↗
94. Ginebra MP, Albuixech L, Fernández-Barragán E et al (2002) Mechanical performance of acrylic bone cements containing different radiopacifying agents. Biomaterials 23:1873–1882. https://doi.org/10.1016/S0142-9612(01)00314-310.1016/S0142-9612(01)00314-3 ↗
95. Chuchulska B, Dimitrova M, Vlahova A et al (2024) Comparative analysis of the mechanical properties and biocompatibility between CAD/CAM and conventional polymers applied in prosthetic dentistry. Polymers (Basel) 16:877. https://doi.org/10.3390/polym1607087710.3390/polym16070877 ↗
96. Hayes G, Laurel M, MacKinnon D et al (2023) Polymers without petrochemicals: sustainable routes to conventional monomers. Chem Rev 123:2609–2734. https://doi.org/10.1021/acs.chemrev.2c0035410.1021/acs.chemrev.2c00354 ↗
97. van Hooy-Corstjens CSJ, Bulstra SK, Knetsch MLW et al (2007) Biocompatibility of a new radiopaque iodine-containing acrylic bone cement. J Biomed Mater Res Part B Appl Biomater 80B:339–344. https://doi.org/10.1002/jbm.b.3060210.1002/jbm.b.30602 ↗
98. Ayre WN, Denyer SP, Evans SL (2014) Ageing and moisture uptake in polymethyl methacrylate (PMMA) bone cements. J Mech Behav Biomed Mater 32:76–88. https://doi.org/10.1016/j.jmbbm.2013.12.01010.1016/j.jmbbm.2013.12.010 ↗
99. Nagaraju N, Kumar VP, Srikanth A et al (2016) Vapor-phase catalytic dehydration of lactic acid to acrylic acid over nano-crystalline cerium phosphate catalysts. Appl Petrochemical Res 6:367–377. https://doi.org/10.1007/s13203-016-0150-510.1007/s13203-016-0150-5 ↗
100. Deka N, Bera A, Roy D, De P (2022) Methyl methacrylate-based copolymers: recent developments in the areas of transparent and stretchable active matrices. ACS Omega 7:36929–36944. https://doi.org/10.1021/acsomega.2c0456410.1021/acsomega.2c04564 ↗