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1.
J Sci Food Agric ; 97(10): 3278-3283, 2017 Aug.
Article in English | MEDLINE | ID: mdl-27976406

ABSTRACT

BACKGROUND: Buckwheat herb is known in the pharmaceutical industry as a material rich in phenolics. Buckwheat is also capable of regrowing and producing an additional harvest in the same year. Although buckwheat herb is a popular material, it is not known whether the regrowth has features of the same quality as the first harvest. Therefore, using the herb of 15 varieties of buckwheat cultivated in Lithuania, the present study aimed to examine biometric properties, phenolic content and antioxidant activity as material quality indicators for buckwheat herb and its regrowth under organic and conventional farming conditions. RESULTS: The highest amount of rutin was indicated in the organically cultivated regrowth of 2015. Buckwheat material accumulated significantly (P < 0.05) lower amounts of other phenolics. A significant correlation between phenolic content and antioxidant activity was observed in the herb and its regrowth in both farming systems. CONCLUSION: Regrowth was of similar quality to the first harvest in terms of phenolic content and antioxidant activity, although a downward trend in several biometric features was observed: the height of the regrowth plants was up to two-fold smaller and biomass was five- to nine-fold lower compared to that of the first harvest plants. Organic and industrial farming systems were determined to produce plants of similar quality. © 2016 Society of Chemical Industry.


Subject(s)
Agriculture/methods , Antioxidants/chemistry , Fagopyrum/chemistry , Fagopyrum/growth & development , Phenols/chemistry , Food, Organic/analysis , Lithuania , Organic Agriculture , Seeds/chemistry , Seeds/growth & development
2.
Addiction ; 107(1): 142-51, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21749526

ABSTRACT

AIMS: To provide controlled data on direct induction with buprenorphine/naloxone (BNX) versus indirect buprenorphine (BPN)-to-BNX induction. DESIGN: Phase 4, prospective, randomized, active-drug controlled, parallel-group trial consisting of a 2-day, double-blind, double-dummy induction phase followed by 26 days of open-label treatment with BNX. SETTING: Nineteen sites in 10 European countries from March 2008 to December 2009. PARTICIPANTS: A total of 187 opioid-dependent men and women ≥ 15 years of age. MEASUREMENTS: The primary objective was assessment of patient response to direct and indirect BNX induction [proportion of patients receiving the scheduled 16-mg BNX dose on day 3 (i.e. first day post-induction)]. Secondary assessments included illicit drug use, treatment retention and compliance, withdrawal scale scores, and safety. FINDINGS: Patient response to direct- versus indirect-BNX induction was similar [direct 91.4% (85/93) versus indirect 90.4% (85/94); 95% confidence interval (CI): -7.3%, 9.2%]. Rapid dose induction (16 mg of BPN equivalent on day 2) was acceptable and 72% of patients completed treatment (day 28). There were no significant differences in secondary measures across groups. An average BNX maintenance dose of 15.3 mg across groups was associated with substantial reductions in illicit opioid use and no self-reported intravenous misuse. Treatment compliance and retention rates were similar (98.5% and 81.3%, respectively). Treatment-emergent adverse event rates were comparable: 75% versus 74% for direct- versus indirect-induction groups, respectively. CONCLUSIONS: Direct buprenorphine/naloxone induction was a safe and effective strategy for maintenance treatment of opioid dependence. Response to high-dose direct buprenorphine/naloxone induction appears to be similar to indirect buprenorphine-to-buprenorphine/naloxone induction and was not associated with reports of intravenous buprenorphine/naloxone misuse.


Subject(s)
Buprenorphine/therapeutic use , Heroin Dependence/drug therapy , Induction Chemotherapy/methods , Naloxone/therapeutic use , Narcotic Antagonists/therapeutic use , Substance Abuse, Intravenous/prevention & control , Administration, Sublingual , Adolescent , Adult , Buprenorphine/administration & dosage , Buprenorphine/adverse effects , Drug Combinations , Europe , Female , Humans , Intention to Treat Analysis , Maintenance Chemotherapy , Male , Middle Aged , Naloxone/administration & dosage , Naloxone/adverse effects , Narcotic Antagonists/administration & dosage , Narcotic Antagonists/adverse effects , Patient Compliance , Prospective Studies , Substance Withdrawal Syndrome/drug therapy , Treatment Outcome , Young Adult
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