Next Article in Journal
The Invasion of the Dwarf Honeybee, Apis florea, along the River Nile in Sudan
Previous Article in Journal
Electrophysiological Responses of Eighteen Species of Insects to Fire Ant Alarm Pheromone

Insects 2019, 10(11), 404;

First Report of Cattle Tick Rhipicephalus (Boophilus) annulatus in Egypt Resistant to Ivermectin
School of Life Science and Engineering, Foshan University, Foshan 528231, China
Faculty of Science, Kafrelsheikh University, Kafr el-Sheikh 33516, Egypt
Department of Parasitology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62515, Egypt
Department of Parasitology, Faculty of Veterinary Medicine, Cairo University, Cairo 11865, Egypt
Authors to whom correspondence should be addressed.
Received: 21 May 2019 / Accepted: 6 September 2019 / Published: 15 November 2019


Tick control is mainly dependent on the application of acaricides, but resistance has developed to almost all classes of acaricides, including macrolactones. Therefore, we aimed to investigate ivermectin resistance among tick populations in middle Egypt. The larval immersion test was conducted using a commercial formulation of ivermectin (1%). Different concentrations of the immersion solution (0.0000625% (625 × 10−7%), 0.000125% (125 × 10−6%), 0.0005% (5 × 10−4%), 0.001% (1 × 10−3%), 0.0025% (2.5 × 10−3%), 0.005% (5 × 10−3), and 0.01% (1 × 10−2%)) were prepared by diluting a commercial ivermectin (1%) with distilled water containing 1% (v/v) ethanol and 2% (v/v) TritonX-100. Field populations of Rhipicephalus annulatus were collected from five different localities in Beni-Suef province, Egypt. Adult engorged female ticks were collected and assessed for oviposition and egg fertility. Eggs were collected, and hatched larvae were then used in the experiment. Application of acaricides was conducted on 10-day-old larvae. There was a significant difference in the LC50 (50% lethal concentration) among the examined localities on the log dose-response plot, where, the LC50 of tick populations from two localities (Emin elaros and Aldiabia) was higher than the other localities (Alhalabia, Alkom, and Beshnna). Besides, tick populations from Emin elaros and Aldiabia showed higher LC90 values with lower slope values compared to those from Alhalabia, Alkom, and Beshnna. According to these values (LC50, LC90, and slope values), as well as a history of acaricide failure to ticks in these areas, R. annulatus developed resistance to ivermectin. This study documents the first report of field populations of R. annulatus resistant to ivermectin in Egypt.
Rhipicephalus annulatus; larval immersion test; ivermectin; resistance

1. Introduction

Hard ticks are the most common cattle ectoparasites that are distributed worldwide. The chemical control of such parasites is mainly through acaricides, which are the primary method used for tick control. However, the widespread use of chemical acaricides has resulted in the selection of acaricide-resistant ticks. Acaricide resistance can be defined as a significant increase in the number of individuals within a tick population that can tolerate doses of acaricides proved to be lethal for the majority of individuals in a sensitive population of the same species [1]. Acaricide resistance continues to be a major obstacle in the control of cattle ticks in many countries, such as Mexico, Australia, and Brazil [2,3]. Ivermectin is one of the macrocyclic lactones (MLs), which are widely used acaricides for controlling tick populations and nematodes. Ticks and nematodes represent the most important constraints to livestock production, particularly in tropical and subtropical areas [4,5]. However, the improper use of macrocyclic lactones has been associated with the development of resistance in populations of ticks worldwide [6,7]. Pharmacokinetics of such compounds (i.e., MLs) in arthropods is well understood by their high affinity to glutamate-gated chloride channels (Glu-Cl) that are found in muscle and nerves. The inhibition of these channels causes a slow and irreversible membrane conductance, resulting in a somatic musculature paralysis and a consequent death of the parasite [8]. Besides, adenosine triphosphate binding cassette (ABC) transporters and esterases play a major role in the detoxification of ivermectin [9]. The early detection of resistance is the target to avoid further selection of resistant ticks using the same active ingredient and to delay the subsequent spread of ivermectin resistance. The larval immersion test (LIT) has been recommended by Food and Agriculture Organization (FAO) as a standard bioassay for testing resistance to MLs [10], which was modified by Klafke et al. [6] and Sabatini et al. [11] to determine 50% and 99.9% lethal concentrations. Several reports have recorded ivermectin resistance in Rhipicephalus microplus populations in Mexico by Perez-Cogollo [12], Uruguay by Castro-Janer [13], and in Brazil by Klafke et al. [6]. In a previous study, we showed that tick populations were resistant to deltamethrin in the same study areas (Beni-Suef, Egypt) [14]. Therefore, this study aimed to evaluate the resistance of field populations of Boophilus annulatus in Beni-Suef province, Egypt, to ivermectin.

2. Materials and Methods

This study was conducted according to the ethical standards of the Faculty of Veterinary Medicine, Beni-Suef University, Egypt, and approved by the Institutional Animal Care and Use Committee of Beni-Suef University (2018-BSUV22).

2.1. Study Area and Data Collection from Farmers

This study was carried out at five different localities, including Alhalabia, Alkom, Beshnna, Aldiabia, and Emin elaros in Beni-Suef province, Egypt (GPS coordinates: 29°04′ N 31°05′ E) (Figure 1). Farmers in these localities were interviewed and questioned to obtain data concerning whether their ivermectin use was mainly as an acaricide or anthelminthic. Furthermore, we queried the farmers as to whether ticks or parasitic worms were more of a problem in their livestock.

2.2. Collection of Ticks and Identification

Fifty engorged females were collected [15] directly from naturally infested cattle in each locality, placed in identified cotton plugged bottles, and transported to the Laboratory of Parasitology, Faculty of Veterinary Medicine, Beni-Suef University for identification under a stereomicroscope using the keys given by Hoogstraal and Kaiser [16] and Walker et al. [17].

2.3. Preparation of R. annulatus larvae

The collected female ticks (R. (B.) annulatus) from a particular area were designated as an isolate. Ticks were thoroughly washed in distilled water, allowed to dry on paper towels, labeled, and incubated individually in separate cotton plugged tubes (2.5 cm diameter) at 27–28 °C with 80–90% relative humidity and a 12-h light/dark cycle for oviposition. After 14 days of egg-laying, the females were discarded, and the number of eggs in each tube was counted. Eggs were hatched within 2 weeks upon removal from the tube. The 10-day-old hatched larvae were ready for testing.

2.4. Preparation of Ivermectin for In Vitro Application

A commercial formulation of ivermectin 1% (Normectin® 1%) was diluted with distilled water containing 1% (v/v) ethanol and 2% (v/v) TritonX-100 solution (Eth-TX) to prepare immersion solutions. Different concentrations of the prepared ivermectin were used (0.0000625% (625 × 10−7%), 0.000125% (125 × 10−6%), 0.0005% (5 × 10−4%), 0.001% (1 × 10−3%), 0.0025% (2.5 × 10−3%), 0.005% (5 × 10−3), and 0.01% (1 × 10−2%)).

2.5. Larval Immersion Test (LIT)

This assay was done in a 1.5 mL microcentrifuge tube, in which 1 mL of each concentration was added. Larvae (200 mg of larvae = 400 larvae) were subsequently added by a paintbrush. A solution without ivermectin was prepared by adding 10 µL of Eth-TX solution to 990 µL of distilled water and served as the control. The tubes, which were closed and vigorously shaken for 15 s, were then gently shaken for 10 min [2]. After treatment, the larvae were transferred to filter paper, dried, then again transferred to a filter paper (8.5 × 7.5 cm), which was folded forming a packet, and closed with ‘‘bulldog’’ clips. These packets were incubated in a biological oxygen demand (BOD) chamber (27–28 °C with 80–90% relative humidity). The mortality rate was determined by counting live and dead larvae (no locomotion). There were triplicates for each concentration.

2.6. Statistical Analysis

Data of the mortality rates were submitted to a Probit analysis. Chi-square test was used to test the hypothesis parallelism and equality (p = 0.05) with Polo-Plus software [18]. Lethal concentrations (LC) for 50% and 90%, with their respective confidence intervals of 95% (CI 95%), were calculated.

3. Results

3.1. History of Ivermectin Use at the Five Study Areas

The survey revealed that 90% of farmers in Aldiabia and Emin elaros areas relied mainly on ivermectin for the treatment of tick infestations. However, farmers in Alhalabia, Alkom, and Beshnna areas used an additional repellent spray in combination with ivermectin injection in heavily infested animals. Furthermore, farmers complained about repeated tick infestation of animals in the study area after a short period from the application of ivermectin (within ~15 days).

3.2. Larval Immersion Test Results

The LC50 and LC90 values for ivermectin with their respective 95% confidence intervals (CI) and slopes for each population are shown in Table 1. The tick population from Aldiabia and Emin elaros areas, which relied on ivermectin treatment, had significantly higher LC50 and LC90 values than the other tick populations. The calculated LC50 (CI 95%) in Emin elaros and Aldiabia areas was 0.0052% (0.0037 to 0.0066) and 0.0051% (0.0046 to 0.0056), respectively. Furthermore, the value was 0.00052% (0.00017 to 0.00088), 0.00029% (0.000062 to 0.000498), and 0.0011% (0.00063 to 0.0015) in Alhalabia, Beshnna, and Alkom areas, respectively (Table 1). The tick populations from Emen elaros and Aldiabia areas could tolerate the higher doses of ivermectin, while those in Alhalabia and Beshnna areas were more susceptible and found dead at lower concentrations of ivermectin. LC90 (CI 95%) was 0.0084%, 0.0011%, 0.0013%, and 0.0027% for tick populations in Aldiabia, Alhalabia, Beshnna, and Alkom areas, respectively (Table 2). The hypothesis of parallelism and equality between regression lines for tick populations from Emen elaros and Aldiabia areas was neglected when compared to tick populations from the other three study areas (Figure 2).

4. Discussion

A few decades ago, the first macrolactones were introduced into the market and continue to be one of the major alternatives for control of bovine parasites, especially in cases of parasites resistant to other chemical groups [19]. R. microplus, which is resistant to macrolactones, has been documented worldwide [6,20]. The dose-response bioassays and/or assessment of the field efficacy of acaricides are the approved methods for confirmation of resistance (FAO, 2004, the World Association for the Advancement of Veterinary Parasitology (WAAVP) [20].
In the present study, various levels of ivermectin susceptibility/resistance in five populations of ticks were reported in Beni-Suef province, Egypt. Two tick populations had the highest LC50, which was 0.0052% and 0.0051% in Emin elaros and Aldiabia, respectively. Due to the lack of a susceptible cattle tick strain (R. annulatus) for comparison, we used published results from previous studies in other countries as reference strains.
The present R. annulatus isolates, which were suspected to be ivermectin resistance, had higher LC50, and their concentration-mortality slopes were similar to the resistant R. microplus tick populations from different areas around the world, including Yucatán [12], Veracruz [15], Sao Paulo [6], and Colombia [6]. A previous study in Mexico [12] indicated that field populations of R. microplus were found to be resistant to ivermectin (i.e., LC50 of these population was higher than that of the susceptible strains, 0.0048). Consequently, the calculated LC50 was 0.00052% and 0.00029% in Alhalabia and Beshnna, respectively, indicating that LC50 was lower than that in the other areas. Moreover, the LC50 in Alkom was higher (0.0011%) than in Alhalabia and Beshanna, indicating that tick populations from Emen elaros and Aldiabia could tolerate the highest dose of ivermectin. Besides, R. annulatus populations from Emen elaros and Aldiabia, which were resistant to ivermectin, had LC90 (0.0092% and 0.0084%) higher than R. annulatus populations from Alhalabia and Beshnna, which were more susceptible and died at lower concentrations of ivermectin (0.001%). Meanwhile, the LC50 for susceptible isolates of R. microplus was reported in different parts of the world, including 3.41 ppm (KUL) in India [21], 5.6 ppm in Germany [22], and 4.2 ppm in Brazil [12]. This is higher than that reported in the present study.
Therefore, the tick populations from Emen elaros and Aldiabia areas were resistant to ivermectin. Additionally, Emin elaros and Aldiabia tick populations exhibited the lowest slope. This result coincides with the results of Klafke [2], who argued that data heterogeneity and low slope were associated with high LC50 and LC90 values, suggesting that many individuals have resistant type allele. A previous study reported that a susceptible strain consisted of completely susceptible individuals and produced the highest slope for the regression line of the dose-response data [12]. Furthermore, it has been stated that low-slopes for the concentration mortality lines, referred as a result of a large heterogeneity with different levels of resistance in the field populations, are studied, and no studies on ivermectin resistant strain have been described with high slopes [6]. The development of R. annulatus resistance to chemicals is influenced by environmental, biological, and management factors that might play crucial roles to generate resistance in the tick populations in Beni-Suef province. However, macrolactones have a more rapid selection of resistant ticks by extending their exposure to sub-therapeutic levels of macrolactones. Intriguingly, R. annulatus has a short life cycle (four tick generations annually) [23]. The latter suggested that R. annulatus might be exposed to acaricides for a long time. The growth of ivermectin resistance has resulted in the widespread use of ivermectin for ectoparasites (ticks) and endoparasites (nematodes), with a broad range of resistance possibility.
The larval immersion test data were matched with the history of ivermectin use at the five study areas. Ivermectin, which is used to control tick and endoparasite infestations, was commonly used in our study sites in Aldiabia and Emenalaros. However, in the other three study areas, ivermectin use is not common. Therefore, the tick populations from Aldiabia and Emenalaros developed resistance to ivermectin. This finding is consistent with findings from San Jeronimo and Tarso farms, Brazil [24], and Colombia [6].

5. Conclusions

In conclusion, R. annulatus resistance to ivermectin is common with different levels in cattle farms in Beni-Suef province, Egypt. However, the intensive use of macrocyclic lactones to control endo- and ectoparasites in the studied area posed more serious complications of ivermectin resistance, failing in terms of treatment and control.

Author Contributions

Conceptualization, S.M.A. and S.E.-A.; Formal analysis, S.E.-A.; Investigation, L.N.M., A.A.K, and M.M.F.; Methodology, L.N.M., A.A.K., and M.M.F.; Supervision, S.M.A.; Writing—review and editing, S.E.-A. and S.M.A.


Start-up Research Grant Program provided by Foshan University, Foshan city, Guangdong province for distinguished researchers, Guangdong Science and Technology Plan Project (Grant No:1244 0600 4560 7389XC), and School of Life Science and Engineering fund (Grant No: KLPREAD201801-02).


The authors appreciate Walid M. Arafa for assistance in result analysis.

Conflicts of Interest

The authors declare no conflict of interest.


  1. Shyma, K.P.; Gupta, J.P.; Singh, V.; Patel, K.K. In Vitro Detection of Acaricidal Resistance Status of Rhipicephalus (Boophilus) microplus against Commercial Preparation of Deltamethrin, Flumethrin, and Fipronil from North Gujarat, India. J. Parasitol. Res. 2015, 2015, 506586. [Google Scholar] [CrossRef] [PubMed]
  2. Klafke, G.M.; Sabatini, G.A.; Thais, A.; Martins, J.R.; Kemp, D.H.; Miller, R.J.; Schumaker, T.T. Larval immersion tests with ivermectin in populations of the cattle tick Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) from State of Sao Paulo, Brazil. Vet. Parasitol. 2006, 142, 386–390. [Google Scholar] [CrossRef] [PubMed]
  3. Aboelhadid, S.M.; Kamel, A.A.; Arafa, W.M.; Shokier, K.A. Effect of Allium sativum and Allium cepa oils on different stages of Boophilus annulatus. Parasitol. Res. 2013, 112, 1883–1890. [Google Scholar] [CrossRef] [PubMed]
  4. El-Ashram, S.; Al Nasr, I.; Abouhajer, F.; El-Kemary, M.; Huang, G.; Dincel, G.; Mehmood, R.; Hu, M.; Suo, X. Microbial community and ovine host response varies with early and late stages of Haemonchus contortus infection. Vet. Res. Commun. 2017, 41, 263–277. [Google Scholar] [CrossRef] [PubMed]
  5. El-Ashram, S.; Al Nasr, I.; El-Kemary, M.; Mehmood, R.; Hu, M.; Suo, X. Early and late gene expression profiles of the ovine mucosa in response to Haemonchus contortus infection employing Illumina RNA-seq technology. Parasitol. Int. 2017, 66, 681–692. [Google Scholar] [CrossRef] [PubMed]
  6. Klafke, G.M.; Castro-Janer, E.; Mendes, M.C.; Namindome, A.; Schumaker, T.T. Applicability of in vitro bioassays for the diagnosis of ivermectin resistance in Rhipicephalus microplus (Acari: Ixodidae). Vet. Parasitol. 2012, 184, 212–220. [Google Scholar] [CrossRef]
  7. Martins, J.R.; Furlong, J. Avermectin resistance of the cattle tick Boophilus microplus in Brazil. Vet. Rec. 2001, 149, 64. [Google Scholar]
  8. Cully, D.F.; Vassilatis, D.K.; Liu, K.K.; Paress, P.S.; Van der Ploeg, L.H.; Schaeffer, J.M.; Arena, J.P. Cloning of an avermectin-sensitive glutamate-gated chloride channel from Caenorhabditis elegans. Nature 1994, 371, 707–711. [Google Scholar] [CrossRef]
  9. Le Gall, V.L.; Klafke, G.M.; Torres, T.T. Detoxification mechanisms involved in ivermectin resistance in the cattle tick, Rhipicephalus (Boophilus) microplus. Sci. Rep. 2018, 8, 12401. [Google Scholar] [CrossRef]
  10. Shaw, R.D. Culture of an organophosphorus-resistant strain of Boophilus microplus (Can.) and an assessment of its resistance spectrum. Bull. Entomol. Res. 1966, 56, 389–405. [Google Scholar] [CrossRef]
  11. Sabatini, G.A.; Kemp, D.H.; Hughes, S.; Nari, A.; Hansen, J. Tests to determine LC50 and discriminating doses for macrocyclic lactones against the cattle tick, Boophilus microplus. Vet. Parasitol. 2001, 95, 53–62. [Google Scholar] [CrossRef]
  12. Perez-Cogollo, L.C.; Rodriguez-Vivas, R.I.; Ramirez-Cruz, G.T.; Miller, R.J. First report of the cattle tick Rhipicephalus microplus resistant to ivermectin in Mexico. Vet. Parasitol. 2010, 168, 165–169. [Google Scholar] [CrossRef] [PubMed]
  13. Castro-Janer, E.; Rifran, L.; Gonzalez, P.; Niell, C.; Piaggio, J.; Gil, A.; Schumaker, T.T. Determination of the susceptibility of Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) to ivermectin and fipronil by Larval Immersion Test (LIT) in Uruguay. Vet. Parasitol. 2011, 178, 148–155. [Google Scholar] [CrossRef] [PubMed]
  14. Aboelhadid, S.M.; Arafa, W.M.; Mahrous, L.N.; Fahmy, M.M.; Kamel, A.A. Molecular detection of Rhipicephalus (Boophilus) annulatus resistance against deltamethrin in middle Egypt. Vet. Parasitol. Reg. Stud. Rep. 2018, 13, 198–204. [Google Scholar] [CrossRef] [PubMed]
  15. Fernández-Salas, A.; Rodríguez-Vivas, R.I.; Alonso-Díaz, M.Á. Resistance of Rhipicephalus microplus to Amitraz and Cypermethrin in Tropical Cattle Farms in Veracruz, Mexico. J. Parasitol. 2012, 98, 1010–1015. [Google Scholar] [CrossRef]
  16. Hoogstraal, H.; Kaiser, M.N. The ticks (Ixodoidea) of Egypt: Abrief review and keys. J. Egypt. Public Health Assoc. 1958, 33, 51–85. [Google Scholar]
  17. Walker, A.R.; Bouattour, A.; Camicas, J.-L.; Estrada-Peña, A.; Horak, I.G.; Latif, A.A.; Pegram, R.G.; Preston, P.M. Ticks of Domestic Animals in Africa: A Guide to Identification of Species; Bioscience Reports: Edinburgh, UK, 2003; p. 157. [Google Scholar]
  18. Abou-Setta, M.M.; Sorrell, R.W.; Childers, C.C. A computer program in basic for determining probit and log-probit or logit correlation for toxicology and biology. Bull. Environ. Contam. Toxicol. 1986, 36, 242–249. [Google Scholar] [CrossRef]
  19. Borges, F.A.; Silva, H.C.; Buzzulini, C.; Soares, V.E.; Santos, E.; Oliveira, G.P.; Costa, A.J. Endectocide activity of a new long-action formulation containing 2.25% ivermectin+1.25% abamectin in cattle. Vet. Parasitol. 2008, 155, 299–307. [Google Scholar] [CrossRef]
  20. Holdsworth, P.A.; Kemp, D.; Green, P.; Peter, R.J.; De Bruin, C.; Jonsson, N.N.; Letonja, T.; Rehbein, S.; Vercruysse, J. World Association for the Advancement of Vet. Parasitol. (WAAVP) guidelines for evaluating the efficacy of acaricides against ticks (Ixodidae) on ruminants. Vet. Parasitol. 2006, 136, 29–43. [Google Scholar] [CrossRef]
  21. Singh, N.K.; Singh, H.; Jyoti, S.H.; Prerna, M.; Rath, S.S. First report of ivermectin resistance in field populations of Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) in Punjab districts of India. Vet. Parasitol. 2015, 214, 192–194. [Google Scholar] [CrossRef]
  22. Chaparro, J.J.; López, A.; Puerta, J.; Villar, D. Ivermectin resistance of three Rhipicephalus microplus populations using the larval immersion test. RCCP Rev. Colomb. Cienc. Pecu. 2016, 29, 51–57. [Google Scholar]
  23. Cen-Aguilar, J.F.; Rodriguez-Vivas, R.I.; Dominguez-Alpizar, J.L.; Wagner, G.G. Studies on the effect of infection by Babesia sp. on oviposition of Boophilus microplus engorged females naturally infected in the Mexican tropics. Vet. Parasitol. 1998, 78, 253–257. [Google Scholar] [CrossRef]
  24. Lopez-Arias, A.; Villar-Argaiz, D.; Chaparro-Gutierrez, J.J.; Miller, R.J.; Perez de Leon, A.A. Reduced Efficacy of Commercial Acaricides Against Populations of Resistant Cattle Tick Rhipicephalus microplus from Two Municipalities of Antioquia, Colombia. Environ. Health Insights 2014, 8, 71–80. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Map of the study area within Beni-Suef province, Egypt. Red dots indicate tick collection sites.
Figure 1. Map of the study area within Beni-Suef province, Egypt. Red dots indicate tick collection sites.
Insects 10 00404 g001
Figure 2. Ivermectin probit mortality × log concentration plots and regression lines of tick populations from the five study areas (Alhalabia, Alkom, Beshnna, Aldiabia, and Eminelaros).
Figure 2. Ivermectin probit mortality × log concentration plots and regression lines of tick populations from the five study areas (Alhalabia, Alkom, Beshnna, Aldiabia, and Eminelaros).
Insects 10 00404 g002
Table 1. Lethal concentration 50 (LC50) and LC90 of 14-day-old larvae treated with ivermectin using a larval immersion test.
Table 1. Lethal concentration 50 (LC50) and LC90 of 14-day-old larvae treated with ivermectin using a larval immersion test.
Location/100 LarvaeSlope (SD) *X2 **t for Slope ***LC50 (95% CI)LC90 (95% CI)
(0.000175 to 0.000881)
(0.00056 to 0.001888)
(0.000062 to 0.000498)
(0.000779 to 0.00188)
(0.000633 to 0.001573)
(0.001585 to 0.003846)
Emin elaros278.37131423.132966.0796590.005189
(0.003788 to 0.006676)
(0.006482 to 0.012057)
(0.004663 to 0.005601)
(0.007669 to 0.009411)
* SD = standard deviation, ** = Chi-square, *** Regression line.
Table 2. The mortality rate of larvae treated with different concentrations of ivermectin in the surveyed areas.
Table 2. The mortality rate of larvae treated with different concentrations of ivermectin in the surveyed areas.
Sample Site
ConcentrationAlkomAlhalabiaBeshnnaAldiabiaEminelaros* p
Ivermectin concentration %0.01100.0 ± 0.0100.0 ± 0.0100.0 ± 0.094.00 ± 2.08287.67 ± 1.4530.0087 **
0.00596.67 ± 0.881999.67 ± 0.3333100.0 ± 0.050.33 ± 1.45354.33 ± 2.3330.0112 *
0.002590.33 ± 1.45398.33 ± 0.881996.67 ± 0.881921.00 ± 2.08227.67 ± 1.4530.0115 *
0.00154.33 ± 2.33390.00 ± 0.091.00 ± 2.0826.667 ± 0.88198.000 ± 1.1550.0138 *
0.000533.33 ± 2.02850.00 ± 0.057.33 ± 1.4535.000 ± 1.1556.667 ± 0.88190.0105 *
0.00012518.67 ± 0.666719.00 ± 1.00044.33 ± 2.3330.3333 ± 0.33331.333 ± 0.88190.0139 *
0.000062510.67 ± 0.66679.333 ± 0.666734.00 ± 2.0820.0 ± 0.00.0 ± 0.00.0093 **
Negative control5 ± 26 ± 35 ± 17 ± 35 ± 2-
All tests were conducted in triplicate; * standard deviation; **, superscript letter is extremely significant.
Back to TopTop