Christopher Johnson Mwankuna

Mr. Christopher Johnson Mwankuna

Department of Chemistry and Physics, Sokoine University of Agriculture, Morogoro, Tanzania
orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 December 2022 in Separations
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Journal Article
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CMChristopher Johnson Mwankuna
Christopher Johnson Mwankuna
EMEliapenda Elisante Mariki
Eliapenda Elisante Mariki
FMFaith Philemon Mabiki
Faith Philemon Mabiki
HMHamisi Masanja Malebo
Hamisi Masanja Malebo
BSBjarne Styrishave
Bjarne Styrishave
RMRobinson Mdegela
Robinson Mdegela
Commercially available conventional drugs have been used to adulterate herbal products. Considering the rapid growth of herbal products’ market, it is essential to screen herbal products for the presence of conventional drugs. Simple analytical methods are needed for the rapid screening of conventional drugs that are likely to be adulterated in herbal products. Thin layer chromatography (TLC) methods for screening twelve conventional drugs in herbal products have been developed and applied. The analytes were extracted from herbal products using acetonitrile:methanol:acetic acid:water (4:4:1:1, v/v). Solvent mixture of dichloromethane:ethyl acetate:methanol (75:15:10, v/v) separated well trimethoprim, sildenafil, paracetamol, and sulfamethoxazole while pyrimethamine, metronidazole, and sulfadoxine were well separated by dichloromethane:ethyl acetate:methanol (77.5:12.5:10, v/v). In addition, acetyl salicylic acid, ibuprofen, diclofenac, quinine, and lumefantrine were well separated by ethyl acetate:methanol:30% ammonia (75:22.5:2.5, v/v). Chromatographic separations were found to be highly reproducible, and more than 10 samples can be analysed in one run. The method was applied in the screening of 229 herbal products. Consequently, 24.0% of the samples contained one adulterant, while 21.4% contained at least two adulterants. All conventional drugs detected in herbal products were not mentioned on the labels and therefore the consumers are kept unaware of their side effects and health problems. Further studies for confirming and quantitatively determining the adulterants in a wide range of products as well as a systematic toxicological analysis of the adulterants in herbal products are recommended.

19 January 2022 in Analytical Methods
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CMChristopher Johnson Mwankuna
Christopher Johnson Mwankuna
GUGrâce Ange Uwamaliya
Grâce Ange Uwamaliya
EMEliapenda Elisante Mariki
Eliapenda Elisante Mariki
FMFaith Mabiki
Faith Mabiki
HMHamisi M. Malebo
Hamisi M. Malebo
BSBjarne Styrishave
Bjarne Styrishave
The use of herbal products adulterated with conventional drugs increases the risk of developing microbial resistance and causes herb-to-drug interaction, leading to severe clinical consequences. The complex nature of herbal products has been a challenge for the unambiguous identification of adulterants. The improved analytical selectivity and sensitivity of hyphenated techniques such as high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) enable the confirmatory screening of adulterants in herbal products. Simultaneous screening of adulterants is necessary and efficient because it has been established that more than one chemical adulterant may be present in one herbal product. An HPLC-MS/MS method for the simultaneous detection and quantification of amoxicillin, ampicillin, metronidazole, ciprofloxacin, sulfamethoxazole, and trimethoprim in powdered herbal drugs was developed. Deuterated metronidazole-d3, trimethoprim-d3, ciprofloxacin-d8, and sulfamethoxazole-d4 were used as internal standards (ISs). For each analyte, two transitions were monitored using protonated molecules as precursor ions. The extraction of analytes from herbal products was performed using a simple methanol : water : formic acid (90 : 10 : 0.05, v/v) extraction solvent. Chromatographic separation was done in a gradient of 0.01% formic acid in methanol and 0.01% formic acid in MilliQ water. The calibration curves were linear (r2 ≥ 0.996) over the range of 0.005–2.5 μg mL−1 for all compounds except metronidazole, whose range was 0.005–1 μg mL−1. The limit of detection (LOD) ranged from 0.012 to 0.046 μg mL−1, while the limit of quantification (LOQ) ranged from 0.066 to 0.153 μg mL−1. The accuracy, expressed as the recovery of spiked herbal products, ranged from 45% to 114%. The precision, expressed as relative standard deviation (RSD) at two concentration levels, ranged from 1.6% to 15.9%. The matrix effect expressed as the matrix factor (MF) ranged from 0.79 to 0.92. The developed method was applied to powder herbal products purchased in Tanzania. Amoxicillin, ampicillin, trimethoprim, sulfamethoxazole, and ciprofloxacin were not detected in all samples. Metronidazole was detected in eight samples with the highest concentration of 1.38 μg g−1. The developed method is suitable for the detection of all the studied antibiotic adulterants in herbal products. Quantification can be performed for all the compounds except ciprofloxacin due to its lower recovery.

24 February 2025 in Next Research
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Journal Article
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RARosemary M. Amiry
Rosemary M. Amiry
CMChristopher Johnson Mwankuna
Christopher Johnson Mwankuna
EMEliapenda Elisante Mariki
Eliapenda Elisante Mariki
SMStelyus L. Mkoma
Stelyus L. Mkoma

9 September 2022 in Chemistry Africa
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Journal Article
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AMA. L. Mpanyakavili
A. L. Mpanyakavili
CMChristopher Johnson Mwankuna
Christopher Johnson Mwankuna
FMF. P. Mabiki
F. P. Mabiki
BSB. Styrishave
B. Styrishave

12 January 2023 in Analytical Sciences
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CMChristopher Johnson Mwankuna
Christopher Johnson Mwankuna
FKFeven Kiros
Feven Kiros
EMEliapenda E. Mariki
Eliapenda E. Mariki
FMFaith P. Mabiki
Faith P. Mabiki
HMHamisi M. Malebo
Hamisi M. Malebo
BSBjarne Styrishave
Bjarne Styrishave