Literature DB >> 27322551

Nanotechnology applied to treatment of mucopolysaccharidoses.

Roselena S Schuh1, Guilherme Baldo2, Helder F Teixeira1.   

Abstract

INTRODUCTION: Mucopolysaccharidoses (MPS) are genetic disorders caused by the accumulation of glycosaminoglycans due to deficiencies in the lysosomal enzymes responsible for their catabolism. Current treatments are not fully effective and are not available for all MPS types. Accordingly, researchers have tested novel therapies for MPS, including nanotechnology-based enzyme delivery systems and gene therapy. In this review, we aim to analyze some of the approaches involving nanotechnology as alternative treatments for MPS. Areas covered: We analyze nanotechnology-based systems, focusing on the biomaterials, such as polymers and lipids, that comprise these nanostructures, and we have highlighted studies that describe their use as enzyme and gene delivery systems for the treatment of MPS diseases. Expert opinion: Some protocols, such as the use of polymer-based systems or nanostructured carriers associated with enzymes and nanotechnology-based carriers for gene therapy, along with combined approaches, seem to be the future of MPS therapy.

Entities:  

Keywords:  Enzyme delivery system; gene therapy; lysosomal storage disorders; mucopolysaccharidoses; nanotechnology

Mesh:

Substances:

Year:  2016        PMID: 27322551     DOI: 10.1080/17425247.2016.1202235

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  8 in total

Review 1.  Hurdles in treating Hurler disease: potential routes to achieve a "real" cure.

Authors:  Brigitte T A van den Broek; Jaap van Doorn; Charlotte V Hegeman; Stefan Nierkens; Caroline A Lindemans; Nanda Verhoeven-Duif; Jaap Jan Boelens; Peter M van Hasselt
Journal:  Blood Adv       Date:  2020-06-23

2.  Nasal Administration of Cationic Nanoemulsions as Nucleic Acids Delivery Systems Aiming at Mucopolysaccharidosis Type I Gene Therapy.

Authors:  Roselena Silvestri Schuh; Juliana Bidone; Edina Poletto; Camila Vieira Pinheiro; Gabriela Pasqualim; Talita Giacomet de Carvalho; Mirian Farinon; Dirnete da Silva Diel; Ricardo Machado Xavier; Guilherme Baldo; Ursula Matte; Helder Ferreira Teixeira
Journal:  Pharm Res       Date:  2018-09-26       Impact factor: 4.200

3.  Neonatal nonviral gene editing with the CRISPR/Cas9 system improves some cardiovascular, respiratory, and bone disease features of the mucopolysaccharidosis I phenotype in mice.

Authors:  Roselena Silvestri Schuh; Esteban Alberto Gonzalez; Angela Maria Vicente Tavares; Bruna Gazzi Seolin; Lais de Souza Elias; Luisa Natalia Pimentel Vera; Francyne Kubaski; Edina Poletto; Roberto Giugliani; Helder Ferreira Teixeira; Ursula Matte; Guilherme Baldo
Journal:  Gene Ther       Date:  2019-12-11       Impact factor: 5.250

4.  A case study of three patients with mucopolysaccharidoses in Hue Central Hospital.

Authors:  Tran Kiem Hao; Nguyen Thi Diem Chi; Nguyen Thi Hong Duc; Nguyen Thi Kim Hoa
Journal:  SAGE Open Med Case Rep       Date:  2020-06-29

5.  Enzyme replacement therapies: what is the best option?

Authors:  Azam Safary; Mostafa Akbarzadeh Khiavi; Rahimeh Mousavi; Jaleh Barar; Mohammad A Rafi
Journal:  Bioimpacts       Date:  2018-07-07

6.  Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases.

Authors:  Edina Poletto; Gabriela Pasqualim; Roberto Giugliani; Ursula Matte; Guilherme Baldo
Journal:  Genet Mol Biol       Date:  2019-05-23       Impact factor: 1.771

Review 7.  Think Big, Start Small: How Nanomedicine Could Alleviate the Burden of Rare CNS Diseases.

Authors:  Abdelfattah Faouzi; Valérie Gaëlle Roullin
Journal:  Pharmaceuticals (Basel)       Date:  2021-01-30

Review 8.  Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses.

Authors:  Rita Barone; Alessandra Pellico; Annarita Pittalà; Serena Gasperini
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

  8 in total

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