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Determination of Glycosaminoglycan Levels by Mass Spectrometry

A glycosaminoglycan and level technology, which is applied in the field of measuring the level of glycosaminoglycans in biological samples, and can solve the problems that quantification or characterization are not easy to achieve.

Active Publication Date: 2019-09-24
TAKEDA PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This is one reason why the quantification or characterization of such GAGs (including HS) is not easy to achieve

Method used

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  • Determination of Glycosaminoglycan Levels by Mass Spectrometry
  • Determination of Glycosaminoglycan Levels by Mass Spectrometry
  • Determination of Glycosaminoglycan Levels by Mass Spectrometry

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0239] Example 1: Liquid chromatography / mass spectrometry (LC / MS) assay for the quantification of heparan sulfate in the cerebrospinal fluid of patients with mucopolysaccharidosis.

[0240] Heparan sulfate was quantified in human cerebrospinal fluid samples by a method for the quantification of heparan sulfate-derived disaccharides in samples using a multi-step protocol. Specifically, the multi-step protocol of this example includes ion-exchange solid-phase extraction, size-exclusion desalting, digestion with heparinase, chemical derivatization, and glycan-specific solid-phase extraction. After glycan-specific solid-phase extraction, use an API 5000 operating in electrospray negative ion mode TM Triple quadrupole mass spectrometer for the analysis of disaccharides by liquid chromatography coupled with tandem mass spectrometry.

[0241] Extraction of HS from CSF

[0242] Diethylaminoethyl (DEAE) resin (175 μL) was added to wells of a 96-well plate with a 20 μm frit. The re...

Embodiment 2

[0319] Example 2: Cerebrospinal fluid heparan sulfate concentrations in untreated Sanfilippo syndrome A patients.

[0320] CSF samples from 25 untreated Sanfilippo syndrome A patients were analyzed using the LC / MS-based HS assay described above. HS concentrations were compared to those of 156 control healthy individuals whose CSF was obtained from a biobank and analyzed using the same method. In the patient group, HS concentrations ranged from 1.94 μM to 9.71 μM, with a mean HS concentration of 4.9 μM ( Figure 6 ). In contrast, 33% of control samples were characterized by HS levels below the lower limit of quantitation (LLOQ) of the assay. Those within the quantifiable range had an average concentration of 0.37 μM, with the lowest and highest concentrations being 0.229 μM and 0.648 μM, respectively. Thus, HS levels in CSF were significantly increased 13-fold in patients with Sanfilippo syndrome A compared with control subjects (t-test; P<0.001).

Embodiment 3

[0321] Example 3: Changes of HS concentration in patients with Sanfilippo syndrome A after intrathecal enzyme replacement therapy.

[0322] This example relates in part to the application of the method of the invention to monitoring patient status and treatment efficacy. Patients with Sanfilippo syndrome A were administered 10 mg, 45 mg, or 90 mg of recombinant heparan N-sulfatase intrathecally monthly for a period of 22 weeks. CSF samples were collected prior to each dose of recombinant heparan N-sulfatase, and HS in CSF was measured using the LC / MS-based HS assay described above. CSF HS changes during the 22-week treatment period as Figure 7 shown. At all doses, the concentration of HS in CSF samples was reduced by 50% relative to baseline (ie, samples collected prior to the first treatment dose). These data show in particular that CSF HS levels remained stable during treatment and that the lowest level of CSFHS was achieved at the 90 mg dose.

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Abstract

Detecting glycosaminoglycans (GAGs) and / or determining the level of one or more glycosaminoglycans can be used, for example, to identify or monitor various medical conditions, the status of patients with various medical conditions, and / or to treat patients with various Response to treatment of patients with medical conditions. The present invention provides methods of detecting glycosaminoglycans and / or determining levels of glycosaminoglycans by using, for example, mass spectrometry.

Description

[0001] Cross References to Related Applications [0002] This application claims priority to US Provisional Patent Application No. 62 / 080,154, filed November 14, 2014, the disclosure of which is incorporated herein in its entirety. Background technique [0003] Various medical conditions are associated with the accumulation of glycosaminoglycans. Glycosaminoglycans (GAGs) are large complex carbohydrate molecules involved in many biological processes. Glycosaminoglycans include polysaccharides derived from hexosamines, such as heparan, heparan sulfate (HS), hyaluronic acid, keratan sulfate, chondroitin sulfate, dermatan sulfate, and copolymers thereof. Various GAGs differ according to, for example, the type of hexosamine, hexose or hexuronic acid units they contain and the geometry of the glycosidic linkages between these units. In some cases, GAG molecules can be broken down into disaccharide components. Given the extent of sulfation, acetylation, epimerization, and other f...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/68C12Q1/34
CPCC12Q1/34G01N33/6893G01N2800/52G01N2800/042G01N2400/40G01N33/6848G01N2560/00
Inventor H·纳伊米Y·邱P·A·J·哈斯利特A·巴比尔
Owner TAKEDA PHARMA CO LTD
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