2020
DOI: 10.1080/17425247.2020.1822320
|View full text |Cite
|
Sign up to set email alerts
|

Preclinical developments of enzyme-loaded red blood cells

Abstract: Introduction: Therapeutic enzymes are currently used in the treatment of several diseases. In most cases, the benefits are limited due to poor in vivo stability, immunogenicity, and drug-induced inactivating antibodies. A partial solution to the problem is obtained by masking the therapeutic protein by chemical modifications. Unfortunately, this is not a satisfactory solution because frequent adverse events, including anaphylaxis, can arise. Area covered: Among the delivery systems, we focused on red blood cel… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
13
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 14 publications
(13 citation statements)
references
References 76 publications
(70 reference statements)
0
13
0
Order By: Relevance
“…In fact, the presence of glucose in the medium fuels the glycolytic pathway, while extracellular methionine at physiological concentrations supports the intracellular production of SAM. Moreover, previous preclinical and clinical studies 10 , 33 on protein-loaded RBCs confirm that engineered erythrocytes maintain a vitality, such as to be a viable therapeutic product, despite some differences existing between untreated native and loaded RBCs, which justify their slightly reduced survival in circulation but do not compromise their therapeutic efficacy. 34 , 35 , 36 The key physiologic mechanisms controlling the in vivo behavior of RBCs engineered as drug delivery system, as well as the design parameters developed to overcome the main critical steps, have been recently reviewed.…”
Section: Discussionmentioning
confidence: 78%
“…In fact, the presence of glucose in the medium fuels the glycolytic pathway, while extracellular methionine at physiological concentrations supports the intracellular production of SAM. Moreover, previous preclinical and clinical studies 10 , 33 on protein-loaded RBCs confirm that engineered erythrocytes maintain a vitality, such as to be a viable therapeutic product, despite some differences existing between untreated native and loaded RBCs, which justify their slightly reduced survival in circulation but do not compromise their therapeutic efficacy. 34 , 35 , 36 The key physiologic mechanisms controlling the in vivo behavior of RBCs engineered as drug delivery system, as well as the design parameters developed to overcome the main critical steps, have been recently reviewed.…”
Section: Discussionmentioning
confidence: 78%
“…Artificial cells containing thymidine phosphorylase can be used to treat mitochondrial neurogastrointestinal encephalomyopathy, and a phase II clinical trial is under development. Additionally, artificial cells containing alcohol oxidase are undergoing preclinical research for alcohol detoxification treatment. …”
Section: Research Status Of Artificial Cellsmentioning
confidence: 99%
“…[ 22 ] A mass of enzymes, proteins, micromolecular drugs, macromolecules, NPs, and even bacteria has been loaded to the surface or interior of erythrocytes, as mentioned in Section 2.1. [ 8,142–144 ] Their applications involve chemo/phototherapy for cancer, [ 15 ] therapeutic delivery for antidotes, [ 145 ] and binding of bacteria to membranes for anti‐infection. [ 142,146 ] They aim to modulate immune responses and to improve and alter pharmacokinetics of therapeutic.…”
Section: Biomedical Applications Of Erythrocyte‐inspired Materialsmentioning
confidence: 99%