Drug Res (Stuttg) 2022; 72(08): 417-423
DOI: 10.1055/a-1886-3208
Review

Dendrimers: A Neuroprotective Lead in Alzheimer Disease: A Review on its Synthetic approach and Applications

Aditya Singh
1   Department of Pharmacy, Integral University, Lucknow, India
,
1   Department of Pharmacy, Integral University, Lucknow, India
,
Tarique Mahmood
1   Department of Pharmacy, Integral University, Lucknow, India
,
Farogh Ahsan
1   Department of Pharmacy, Integral University, Lucknow, India
,
Rufaida Wasim
1   Department of Pharmacy, Integral University, Lucknow, India
› Author Affiliations

Abstract

Alzheimer disease is a neurodegenerative disease that is signified by cognitive decline, memory loss, and erratic behavior. Dendrimers are a type of polymer that has a well-defined structure, a high degree of molecular uniformity, and a low polydispersity which have shown to be effective intracellular drug carriers for bring down the in numerous cases. The data reported by the clinical trials and chemical bonds of dendrimers loading and biological properties that may be used in the bringing out the treatment of nano formulation for Alzheimer disease. Below-range dendrimers have an unlocked figure, but higher-range dendrimers have a more globular and dense structure so handling is difficult. Dendrimers are similar in size to a variety of biological structures; for example, fifth-generation polyamidoamine (PAMAM) dendrimers are similar in size and shape to haemoglobin (5.5 nm diameter). Each generation of dendrimer is described in terms of size, shape, molecular weight, and the number of surface functional groups, with increasing growth specified in terms of 'generation number.' In contrast, Hawker and Frechet were the first to report the convergent approach. A stepwise repeating reaction strategy is used to synthesize dendrimers radically from a central core. The value of dendrimers as drug carriers is discussed in this paper. The information presented in this article can provide useful references for further studies on making dendrimers and applications.



Publication History

Received: 28 April 2022

Accepted: 27 June 2022

Article published online:
05 August 2022

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Benters R, Niemeyer CM, Drutschmann D. et al. DNA microarrays with PAMAM dendritic linker systems. Nucleic acids research 2002; 30: e10-e10
  • 2 Barceló D, Farré M. (Eds.). Analysis and risk of nanomaterials in environmental and food samples (Vol. 59). Newnes; 2012
  • 3 Abbasi E, Aval SF, Akbarzadeh A. et al. Dendrimers: synthesis, applications, and properties. Nanoscale research letters 2014; 9: 1-10.
  • 4 Balzani V, Ceroni P, Gestermann S. et al. Dendrimers as fluorescent sensors with signal amplification. Chemical Communications 2000; 10: 853-854
  • 5 Tomalia DA, Baker H, Dewald J. et al. A new class of polymers: starburst-dendritic macromolecules. Polymer journal 1985; 17: 117-132
  • 6 Liu MJ, Fréchet JMJ. Preparation of water-soluble dendritic unimolecular micelles as potential drug delivery agents. In Abstracts of papers of the american chemical society (Vol. 217, pp. U452-U452). 1155 16th ST, NW, Washington, DC 20036 USA: Amer chemical soc (1999, March)
  • 7 Buhleier E, Wehner W, Vögtle F. Cascade′-and′ Nonskid-Chain-like′ syntheses of molecular cavity topologies. Chemischer Informationsdienst 1978; 9: 155-158
  • 8 Naylor AM, Goddard WA, Kiefer GE. et al. Starburst dendrimers. 5. Molecular shape control. Journal of the American Chemical Society 1989; 111: 2339-2341
  • 9 Hong S, Bielinska AU, Mecke A. et al. Interaction of poly (amidoamine) dendrimers with supported lipid bilayers and cells: hole formation and the relation to transport. Bioconjugate chemistry 2004; 15: 774-782
  • 10 Venuganti VVK, Perumal OP. Poly (amidoamine) dendrimers as skin penetration enhancers: Influence of charge, generation, and concentration. Journal of pharmaceutical sciences 2009; 98: 2345-2356
  • 11 Burnette RR, Ongpipattanakul B. Characterization of the permselective properties of excised human skin during iontophoresis. Journal of pharmaceutical sciences 1987; 76: 765-773
  • 12 Mishra V, Gupta U, Jain NK. (2009). Surface-engineered dendrimers: a solution for toxicity issues. Journal of Biomaterials Science, Polymer Edition 2009; 20: 141-166
  • 13 Boas U, Heegaard PM. Dendrimers in drug research. Chemical Society Reviews 2004; 33: 43-63
  • 14 Pittman C. Column: Polymer Supports in Synthesis. Polymer News 2004; 29: 213-214
  • 15 Chapman TM, Hillyer GL, Mahan EJ. et al. (1994). Hydraamphiphiles: novel linear dendritic block copolymer surfactants. Journal of the American Chemical Society 1994; 116: 11195-11196
  • 16 D'Emanuele A, Attwood D. Dendrimer–drug interactions. Advanced drug delivery reviews 2005; 57: 2147-2162
  • 17 Devadoss C. Electroactive and Photoactive Dendrimers. In Supramolecular Photosensitive and Electroactive Materials (pp. 793-858 Academic Press; 2001
  • 18 Duncan R, Izzo L. Dendrimer biocompatibility and toxicity. Advanced drug delivery reviews 2005; 57: 2215-2237
  • 19 Esfand R, Tomalia DA. Poly (amidoamine) (PAMAM) dendrimers: from biomimicry to drug delivery and biomedical applications. Drug discovery today 2001; 6: 427-436
  • 20 Fu HL, Cheng SX, Zhang XZ. et al. Dendrimer/DNA complexes encapsulated functional biodegradable polymer for substrate-mediated gene delivery. The Journal of Gene Medicine: A cross-disciplinary journal for research on the science of gene transfer and its clinical applications 2008; 10: 1334-1342
  • 21 Gajbhiye V, Kumar PV, Sharma A. et al. Novel PEGylated PPI dendritic nanostructures for sustained delivery of anti-inflammatory agent. Current Nanoscience 2008; 4: 267-277
  • 22 Hawker CJ, Frechet JM. Preparation of polymers with controlled molecular architecture. A new convergent approach to dendritic macromolecules. Journal of the American Chemical Society 1990; 112: 7638-7647
  • 23 Heneka MT, O'Banion MK. Inflammatory processes in Alzheimer's disease. Journal of neuroimmunology 2007; 184: 69-91
  • 24 Jadoopat R. Review of Alzheimer’s disease treatment and potential future therapies. Annual Review of Changes in Healthcare 2018; 2: 1
  • 25 Jansen JF, Meijer E, De Brabander-Van Den Berg EM. Bengal rose@ dendritic box. In Macromolecular Symposia (1996, January). (Vol. 102, No. 1, pp. 27-33 Basel: Hüthig & Wepf Verlag;
  • 26 Kateb B, Chiu K, Black KL. et al. Nanoplatforms for constructing new approaches to cancer treatment, imaging, and drug delivery: what should be the policy?. Neuroimage 2011; 54: S106-S124
  • 27 Khoee S, Hemati K. Synthesis of magnetite/polyamino-ester dendrimer based on PCL/PEG amphiphilic copolymers via convergent approach for targeted diagnosis and therapy. Polymer 2013; 54: 5574-5585
  • 28 Kojima C, Kono K, Maruyama K. et al. Synthesis of polyamidoamine dendrimers having poly (ethylene glycol) grafts and their ability to encapsulate anticancer drugs. Bioconjugate chemistry 2000; 11: 910-917
  • 29 Koppu S, Oh YJ, Edrada-Ebel R. et al. Tumor regression after systemic administration of a novel tumor targeting gene delivery system carrying a therapeutic plasmid DNA. J. Control. Release. 2010; 143: 215-221
  • 30 Lee JW, Choi SP, Thiruvenkatachari R. et al. Submerged microfiltration membrane coupled with alum coagulation/powdered activated carbon adsorption for complete decolorization of reactive dyes. Water research 2006; 40: 435-444
  • 31 Liu M, Fréchet JM. Designing dendrimers for drug delivery. Pharmaceutical science & technology today 1999; 2: 393-401
  • 32 Mourey TH, Turner SR, Rubinstein M. et al. Unique behavior of dendritic macromolecules: intrinsic viscosity of polyether dendrimers. Macromolecules 1992; 25: 2401-2406
  • 33 Newkome GR, Moorefield CN, Vögtle F. et al. Dendrimers and dendrons: concepts, syntheses, applications. 2001. 623. Weinheim: Wiley-vch;
  • 34 Ooya T, Lee J, Park K. Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel. Journal of controlled release 2003; 93: 121-127
  • 35 Ottaviani MF, Cossu E, Turro NJ. et al. Characterization of starburst dendrimers by electron paramagnetic resonance. 2. Positively charged nitroxide radicals of variable chain length used as spin probes. Journal of the American Chemical Society 1995; 117: 4387-4398
  • 36 Pan G, Lemmouchi Y, Akala EO. et al. Studies on PEGylated and drug-loaded PAMAM dendrimers. Journal of bioactive and compatible polymers 2005; 20: 113-128
  • 37 Patel HN, Patel PM. Dendrimer applications – A review. Int J Pharm Bio Sci 2013; 4: 454-463
  • 38 Pearson S, Jia H, Kandachi K. China approves first gene therapy. Nature biotechnology 2004; 22: 3-4 DOI: 10.1038/nbt0104-3.
  • 39 Sadekar S, Ghandehari H. Transepithelial transport and toxicity of PAMAM dendrimers: implications for oral drug delivery. Advanced drug delivery reviews 2012; 64: 571-588
  • 40 Schultz LG, Zhao Y, Zimmerman SC. Synthesis of Cored Dendrimers with Internal Cross-Links. Angewandte Chemie International Edition 2001; 40: 1962-1966
  • 41 Seabrook TJ, Thomas L, Lemere K. et al. Boosting with intranasal dendrimeric Aβ 1-15 but not Aβ1-15 peptide leads to an effective immune response following a single injection of Aβ1-40/42in APP-Tg mice. J. Neuroinflammation. 2006; 3: 14
  • 42 Sevenson S, Tomalia DA. Dendrimers in biomedical applications –reflections on the field. Advanced drug delivery reviews 2012; 64: 102-115
  • 43 Valdes Lizama O, Vilos C, Durán-Lara E. Techniques of structural characterization of dendrimers. Current Organic Chemistry 2016; 20: 2591-2605
  • 44 Yiyun C, Na M, Tongwen X. et al. Transdermal delivery of nonsteroidal anti-inflammatory drugs mediated by polyamidoamine (PAMAM) dendrimers. Journal of pharmaceutical sciences 2007; 96: 595-602
  • 45 Zhang GD, Harada A, Nishiyama N. et al. Polyion complex micelles entrapping cationic dendrimer porphyrin: effective photosensitizer for photodynamic therapy of cancer. Journal of controlled release 2003; 93: 141-150