Glucosamine Hydrochloride

2010 ◽  
Vol 33 (2) ◽  
pp. 293-299 ◽  
Author(s):  
In Hee Han ◽  
Sung-Up Choi ◽  
Dae Young Nam ◽  
Young Mi Park ◽  
Myung Joo Kang ◽  
...  

2013 ◽  
Vol 455 (1-2) ◽  
pp. 365-373 ◽  
Author(s):  
Shuai Qian ◽  
Qizhi Zhang ◽  
Yanfeng Wang ◽  
Benjamin Lee ◽  
Guru V. Betageri ◽  
...  

1970 ◽  
Vol 46 (3) ◽  
pp. 375-378 ◽  
Author(s):  
MM Islam ◽  
SM Masum ◽  
MM Rahman ◽  
AA Shaikh

The present investigation described the effective preparation of glucosamine hydrochloride (GluHCl) from chitin which was extracted from indigenous shrimp shell. GluHCl has attracted much attention owing to its therapeutic activity in osteoarthritis and widely used dietary supplement. The key step involved was extraction of chitin from shrimp skeleton and then hydrolysis of chitin by concentrated hydrochloric acid. The reaction proceeds via break down of glycoside linkage. Structural analysis was carried out by melting point, TLC, FT-IR, elemental analysis and all the data were compared with that of standard GluHCl. The elemental (C, 32.75; H, 6.51; N, 6.20) analysis is good concord with the calculated value (C, 33.42; H, 6.54; N, 6.50). Absence of v max at 1726 cm-1 indicates that GluHCl is a deacetylated product of chitin. The yields of the product mainly depend on reaction conditions. Maximum yield (63.5%) was obtained when chitin was hydrolyzed with concentrated HCl for 1.30 h. Key words: Shrimp shell; Chitin, Acid hydrolysis; Glucosamine hydrochloride Osteoarthritis. DOI: http://dx.doi.org/10.3329/bjsir.v46i3.9046 BJSIR 2011; 46(3): 375-378


2019 ◽  
Vol 72 (2) ◽  
pp. 193-197
Author(s):  
Kyrylo V. Makolinets ◽  
Vasyl I. Makolinets ◽  
Dmytro V. Morozenko ◽  
Kateryna V. Gliebova ◽  
Svitlana I. Danylchenko

Introduction: There are many methods for diagnosis and treatment of knee joints osteoarthritis in modern orthopedics. The infrared radiation is one of the most popular and effective methods though it needs experimental substantiation on rats. The aim: Experimental definition of the effectiveness of the proposed method of conservative treatment of knee joints osteoarthritis using sodium diclofenac, glucosamine hydrochloride and infrared laser radiation, on the basis of biochemical markers of connective tissue metabolism in rats. Materials and methods: Experimental studies were performed on 40 white male rats. A part of rats received infrared laser radiation in addition to diclofenac sodium and glucosamine hydrochloride. Results: Using a complex of infrared laser radiation and glucosamine hydrochloride and diclofenac sodium in conservative treatment of rats with experimentally induced knee joints osteoarthritis rats after 24 days of treatment. Treatment with the above-mentioned scheme resulted in a significant reduction in the content of glycoproteins (28.5%), chondroitin sulfates (26.1%), alkaline phosphatase activity (32.3%), and I and II fractions of glycosaminoglycans, namely chondroitin-6- (28.7%) and chondroitin-4-sulfate (40.3%). Moreover, these indicators of the studied markers approached the level of intact animals. Conclusions: Changes in biochemical markers of connective tissue in rats during experimental knee joints osteoarthritis indicated a higher efficiency of the treatment regimen with the use of low-intensity infrared laser radiation compared with exclusively drug therapy.


The behaviour of the albumin glucosides and the mucus bodies known as mucins, mucinogens, mucoids , and hyalogens , on hydrolysis suggests the probability that these complex proteins would bear the same relation to the condensation products of the sugars or the amino-sugars with the amino-acids as the simpler proteins bear to the polypeptides. Consequently, the authors decided two years ago to make a start in the synthesis of the glucoproteins by preparing the condensation products of glucosamine with the amino-aliphatic acids, in order that their properties and behaviour towards ferments could be ascertained and compared with those of the degradation products of the glucoproteins and thereby throw some light on the constitution of these complex and important organic bodies. After many failures, the method of synthesis which we eventually adopted for the condensation of glucosamine with amino-aliphatic acids was somewhat similar to one of the methods employed by Emil Fischer and his co-workers in the synthesis of the polypeptides. In brief, the method consists in condensing α -bromoacyl haloids with glucosamine hydrochloride in the presence of sodium hydroxide, and then displacing the halogen in the resulting α -bromoacyl glucosamines by an amino-group through the action of cold aqueous ammonia, viz:- α -Bromoacyl Haloid + Glucosamine Hydrochloride. sodium ↓ hydroxide. α -Bromoacyl Glucosamine. aqueous ↓ ammonia. Anhydride of α -Aminoacyl Glucosamine.


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