The identities and anti-herpes simplex virus activity of Clinacanthusnutans and Clinacanthus siamensis

Objective: To distinguish the difference among the Clinacanthus nutans (Burm. f.) Lindau (C. nutans) and Clinacanthus siamensis Bremek (C. siamensis) by assessing pharmacognosy characteristics, molecular aspect and also to evaluate their anti-herpes simplex virus (HSV) type 1 and type 2 activities. Methods: Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline. Stomatal number, stomatal index and palisade ratio of leaves were evaluated. Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PCR and then sequenced. Dry leaves were subsequently extracted withn-hexane, dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay. Results: Cross section of midrib and stem showed similar major components. Leaf measurement index of stomatal number, stomatal index and palisade ratio of C. nutans were 168.32±29.49, 13.83±0.86 and 6.84±0.66, respectively, while C. siamensis were 161.60±18.04, 11.93±0.81 and 3.37±0.31, respectively. The PCR amplification of ITS region generated the PCR product approximately 700 bp in size. There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions. The IC50 values of C. nutans extracted with n-hexane, dichloromethane and methanol against HSV-1 were (32.05±3.63) μg/mL, (44.50±2.66) μg/mL, (64.93±7.00) μg/mL, respectively where as those of C. siamensis were (60.00±11.61) μg/mL, (55.69±4.41) μg/mL, (37.39±5.85) μg/mL, respectively. Anti HSV-2 activity of n-hexane, dichloromethane and methanolC. nutans leaves extracts were (72.62±12.60) μg/mL, (65.19±21.45) μg/mL, (65.13±2.22) μg/mL, respectively where as those of C. siamensis were (46.52±4.08) μg/mL, (49.63±2.59) μg/mL, (72.64±6.52) μg/mL, respectively. Conclusions: The combination of macroscopic, microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent.

The identities and anti-herpes simplex virus activity of Clinacanthus nutans and Clinacanthus siamensis

<p><b>OBJECTIVE</b>To distinguish the difference among the Clinacanthus nutans (Burm. f.) Lindau (C. nutans) and Clinacanthus siamensis Bremek (C. siamensis) by assessing pharmacognosy characteristics, molecular aspect and also to evaluate their anti-herpes simplex virus (HSV) type 1 and type 2 activities.</p><p><b>METHODS</b>Macroscopic and microscopic evaluation were performed according to WHO Geneva guideline. Stomatal number, stomatal index and palisade ratio of leaves were evaluated. Genomic DNA was extracted by modified CTAB method and ITS region was amplified using PCR and then sequenced. Dry leaves were subsequently extracted with n-hexane, dichloromethane and methanol and antiviral activity was performed using plaque reduction assay and the cytotoxicity of the extracts on Vero cells was determined by MTT assay.</p><p><b>RESULTS</b>Cross section of midrib and stem showed similar major components. Leaf measurement index of stomatal number, stomatal index and palisade ratio of C. nutans were 168.32±29.49, 13.83±0.86 and 6.84±0.66, respectively, while C. siamensis were 161.60±18.04, 11.93±0.81 and 3.37±0.31, respectively. The PCR amplification of ITS region generated the PCR product approximately 700 bp in size. There were 34 polymorphisms within the ITS region which consisted of 11 Indels and 23 nucleotide substitutions. The IC50 values of C. nutans extracted with n-hexane, dichloromethane and methanol against HSV-1 were (32.05±3.63) µg/mL, (44.50±2.66) µg/mL, (64.93±7.00) µg/mL, respectively where as those of C. siamensis were (60.00±11.61) µg/mL, (55.69±4.41) µg/mL, (37.39±5.85) µg/mL, respectively. Anti HSV-2 activity of n-hexane, dichloromethane and methanol C. nutans leaves extracts were (72.62±12.60) µg/mL, (65.19±21.45) µg/mL, (65.13±2.22) µg/mL, respectively where as those of C. siamensis were (46.52±4.08) µg/mL, (49.63±2.59) µg/mL, (72.64±6.52) µg/mL, respectively.</p><p><b>CONCLUSIONS</b>The combination of macroscopic, microscopic and biomolecular method are able to authenticate these closely related plants and both of them have a potency to be an anti-HSV agent.</p>

Simultaneous detection of amphetamine, methamphetamine and ephedrine by heterology competitive enzyme-linked immunosorbent assay

Background: Simultaneous screening of ephedrine with amphetamine or methamphetamine in drug abusers is useful in countries, such as Thailand, that prohibit the use of ephedrine. The lack of an adequate screening test kit suitable for this purpose is a significant obstacle in the detection of ephedrine abusers. A reliable analytical method for the simultaneous detection of amphetamine, methamphetamine and ephedrine is needed. Objective: To develop a process for the detection of amphetamine, methamphetamine and ephedrine by enzyme-linked immunosorbent assay (ELISA), based on the polyclonal antibody and heterology principle. Methods: The 3-aminopropyl (3AP) and 4-aminobutyl (4AB) derivatives of amphetamine (A), methamphetamine (M) and ephedrine (E) were chemically synthesized. They were used for the preparations of immunogens and hapten tracers. Direct competitive ELISA of matrix combinations of antisera and hapten tracers were performed using amphetamine, methamphetamine and ephedrine as the analytes. Only the competitive reactions with specified sensitivity and specificity are selected. Results: The study discovered three assay combinations that demonstrated concentration-dependent competition of analyte (single or multiple). They passed the confirmation test for the cut-off concentration and had no cross-reactivity with other amines or structured related compounds. The assay combinations of 4ABA-Ab with 3APA-PO and 4ABE-Ab with 3APM-PO were specific for the detection of amphetamine with ephedrine and methamphetamine with ephedrine, respectively. The third assay combination of 4ABE-Ab with 3APE-PO was highly specific to ephedrine with negligible cross-reactivity from other structure-related compounds. Direct competitive ELISA of 4ABE-Ab with 3APM-PO has been proven useful in field tests for the detection of methamphetamine in urine samples from Thai truck drivers suspected of drug abuse. Conclusion: By using heterology, these three assay combinations could be used separately or simultaneously for drug abuse screening.