Study of the l-Phenylalanine Ammonia-Lyase Penetration Kinetics and the Efficacy of Phenylalanine Catabolism Correction Using In Vitro Model Systems.
biomedical drug
catabolism disorder
enzyme
kinetics
l-phenylalanine ammonia-lyase
phenylketonuria
Journal
Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003
Informations de publication
Date de publication:
13 Mar 2021
13 Mar 2021
Historique:
received:
21
02
2021
revised:
10
03
2021
accepted:
11
03
2021
entrez:
3
4
2021
pubmed:
4
4
2021
medline:
4
4
2021
Statut:
epublish
Résumé
The kinetics of l-phenylalanine ammonia-lyase (PAL) penetration into the monolayer of liver cells after its release from capsules was studied. The studies showed the absence of the effect of the capsule shell based on plant hydrocolloids on the absorption of l-phenylalanine ammonia-lyase in systems simulating the liver surface. After 120 min of incubation, in all variants of the experiment, from 87.0 to 96.8% of the enzyme penetrates the monolayer of liver cells. The combined analysis of the results concludes that the developed encapsulated form of l-phenylalanine ammonia-lyase is characterized by high efficiency in correcting the disturbed catabolism of phenylalanine in phenylketonuria, which is confirmed by the results of experiments carried out on in vitro model systems. PAL is approved for the treatment of adult patients with phenylketonuria. The encapsulated l-phenylalanine ammonia-lyase form can find therapeutic application in the phenylketonuria treatment after additional in vitro and in vivo studies, in particular, the study of preparation safety indicators. Furthermore, it demonstrated high efficacy in tumor regression and the treatment of tyrosine-related metabolic disorders such as tyrosinemia. Several therapeutically valuable metabolites biosynthesized by PAL via its catalytic action are included in food supplements, antimicrobial peptides, drugs, amino acids, and their derivatives. PAL, with improved pharmacodynamic and pharmacokinetic properties, is a highly effective medical drug.
Identifiants
pubmed: 33805682
pii: pharmaceutics13030383
doi: 10.3390/pharmaceutics13030383
pmc: PMC7999051
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Russian Foundation for Basic Research
ID : 18-08-00444
Références
Plant Physiol Biochem. 2017 Sep;118:413-421
pubmed: 28711790
Sci Rep. 2020 Jan 28;10(1):1315
pubmed: 31992763
Biomolecules. 2020 May 30;10(6):
pubmed: 32486192
J Am Diet Assoc. 2008 Oct;108(10):1704-7
pubmed: 18926138
Mol Genet Metab. 2010;99 Suppl 1:S64-7
pubmed: 20123473
Mol Genet Metab. 2018 Aug;124(4):223-229
pubmed: 29941359
Pharmaceuticals (Basel). 2020 Apr 09;13(4):
pubmed: 32283743
Sci Rep. 2019 Dec 27;9(1):20123
pubmed: 31882791
Food Technol Biotechnol. 2016 Sep;54(3):296-303
pubmed: 27956861
J Clin Invest. 1999 Apr;103(8):1169-78
pubmed: 10207169
Phytochemistry. 2015 Sep;117:90-97
pubmed: 26070140
Hum Gene Ther. 2010 Apr;21(4):463-77
pubmed: 19916803
Nat Biotechnol. 2018 Oct;36(9):857-864
pubmed: 30102294
Chem Commun (Camb). 2020 May 14;56(39):5255-5258
pubmed: 32270162
Biochem J. 2000 Apr 1;347 Pt 1:1-16
pubmed: 10727395
Plant J. 2017 Dec;92(5):939-950
pubmed: 28977710
Sci Rep. 2020 Feb 27;10(1):3651
pubmed: 32107425
Plants (Basel). 2020 Apr 09;9(4):
pubmed: 32283640
Mol Ther. 2004 Aug;10(2):220-4
pubmed: 15294168
Chem Rev. 2018 Jan 10;118(1):73-118
pubmed: 28497955
Heliyon. 2019 Dec 27;6(1):e03096
pubmed: 31909265
J Med Genet. 1995 Dec;32(12):976-8
pubmed: 8825928
Toxicol In Vitro. 2009 Oct;23(7):1387-95
pubmed: 19631733