Skip to main content
  • Research article
  • Open access
  • Published:

Microbial contamination in herbal medicines: a serious health hazard to elderly consumers

Abstract

Introduction

The use of herbal medicine is on the rise worldwide, and safety issues associated with herbal medicines may have an exacerbated impact in elderly because this population has an increased susceptibility and sensitivity to health complications due to the aging process.

Methods

This cross-sectional study was carried out at a primary health care unit in the city of Macapa, Brazil. The herbal medicines used and the sociodemographic characteristics of 123 voluntarily consenting participants were collected using a structured questionnaire. A total of 132 herbal medicines with oral or topical administration were donated by the elderly for microbial analysis before consumption, and 18 water samples used in the preparation of homemade herbal medicines were collected. Bacterial and fungal counts and identification of bacterial pathogens (Escherichia coli, Salmonella spp., Pseudomonas aeruginosa and Staphylococcus aureus) were performed according to the regulations of the Brazilian Pharmacopoeia and World Health Organization. Water analysis for the detection of coliforms and E. coli was carried out using Colilert® according to the manufacturer’s instructions and the techniques established by Standard Methods.

Results

Of the study participants, 78.8% were women. Bacterial growth was observed in samples from 51.5% of study and 35.6% had fungal growth. A total of 31.8% of the herbal medicine samples exceeded the safety limits (CFU/g ≤ 105), including 16.7% of the homemade herbal medicines and 15.1% of the commercial herbal medicines. It was also found that 31.0% of the samples exceeded the safety limit for fungal growth. The microorganisms most commonly isolated from the herbal medicines were S. aureus (49.2%), followed by Salmonella spp. (34.8%), E. coli (25.8%), and P. aeruginosa (14.4%). Of water samples analyzed, 77.8% were positive for total coliforms (1 ml) and in 66.7% water samples E. coli was detected (1 ml), making them unfit for consumption.

Conclusions

The use of homemade and commercial herbal medicines is a major risk to the health of elderly who use these therapies due to the lack of microbial quality standards. We observed levels of viable bacteria and fungi that were above safety limits; in addition, we were able to isolate pathogenic bacteria from these herbal medicines.

Peer Review reports

Background

It is estimated that approximately 80% of the population in developing countries uses traditional herbal medicines as part of their primary health care [1, 2]. This finding highlights the importance of research to support the development of traditional herbal medicine practices that provide appropriate, safe, and effective treatments [2,3,4]. Among the main safety risks related to herbal medicines is contamination by microorganisms of various kinds that may be adherent to leaves, stems, flowers, seeds, and roots from which herbal medicines are prepared. Alternatively, microorganisms can be introduced during harvesting, handling, open-air drying, preserving, and manufacturing [4,5,6].

Because of gradual devaluation of the knowledge associated with traditional health care-related practices [7], health surveys conducted in several countries have demonstrated the use of herbal medicines as a mainstream practice among elderly people compared with that among young adults [8]. According to the World Health Organization (WHO) [9], the definition of “elderly people” is established according to the socioeconomic level of each nation, with elderly individuals defined as being 60 years of age or greater in developing countries, while in developed countries, the age limit extends to 65 years.

The risk of microbial contamination may have an exacerbated impact in the elderly population because this population has increased susceptibility to the consumption of herbal medicines and sensitivity to health complications due to the aging process. The aging process, according to some studies [10,11,12], is characterized by morphological changes and physiological, biochemical and psychological factors that lead to a decrease in an individual’s ability to adapt to the environment.

Thus, it is important to consider the health care needs of this population. The prevalence of acute and chronic diseases increases with aging. This increase also leads to a considerable increase in the consumption of medications, and these factors predispose the geriatric population to the risks of polypharmacy as well as an increased occurrence of adverse events [13]. As a result, the presence of microbial contaminants in herbal products can adversely affect the health status of consumers due to their immunocompromised conditions and microbial infections, creating a health problem throughout the world. Therefore, the safety of consumers of herbal products is of the utmost importance [14], especially in elderly populations.

In the Brazilian Amazon, there is substantial consumption of herbal medicines due to cultural, social, and economic factors as well as the availability of a vast biodiversity of regional flora. However, there is no sufficient data that address the microbial quality of these herbal medicines. The present study evaluated the microbial quality (quantification of aerobic bacteria, identification of pathogenic bacteria and determination of presence of fungi) of herbal medicines (commercial and homemade) and of water used in the preparation of homemade herbal medicines consumed by the elderly population in the Brazilian Amazon (Macapa, Amapa State).

Methods

Study area, design and period

This cross-sectional study was carried out from May 1, 2016 to October 1, 2017 at the Frei Daniel Samarate primary health care unit in the city of Macapa, which is located in northern Brazil (latitude 00°02′18.84“N and longitude 51°03’59.10”W). The town has an estimated area of 6.503.458 km2, with a population of over 398.204, of which 20.508 are elderly individuals [15]. Macapa is situated on a small plateau in the Amazon in the southeast of the state of Amapa and has few land connections with other parts of Brazil.

Source of population and study subjects

All types of herbal medicines used by the 123 voluntary participants were used as the study subjects. It was compulsory that these people were at least 60 years of age, nonindigenous (to establish ethical criteria because studies involving indigenous people and their knowledge/culture are required to follow specific ethical recommendations), and in perfect mental health (certified through the analysis of medical records). Sociodemographic characteristics were also collected using a structured questionnaire.

Sample size and sampling technique

In the present study, a total of 132 (86 liquid, 25 semisolid and 13 solid) herbal medicines with an oral or topical administration were donated for microbial analysis by the 123 elderly participants before consumption. The samples were sold at different markets in the town of Macapa (commercial/industrialized or technically elaborated product) or prepared by the elderly individuals themselves (homemade/herbalists). A total of 18 water samples used in the preparation of herbal medicines by participants (homemade) were included as study subjects.

Inclusion and exclusion criteria

Liquid, semisolid or solid preparations of herbal medicinal products administered orally or topically with or without further pharmaceutical processing stored in their original container (in the case of commercial products) or collected in sterile bottles provided by the researchers (in the case of homemade herbal medicines) were included in the study. Herbal medicines with other routes of administration and/or those that were delivered in unsuitable bottles (nonsterile or different from the original) were excluded from the study.

Data collection and handling and transportation of specimens

Using aseptic techniques, 10 mL (liquid) or 10 g (semisolid or solid) of samples from each herbal preparation were collected using a sterile screw-capped bottle. Eighteen water samples used to prepare liquid herbal medicines were collected by immersing a 100-mL sterile screw-capped bottle in a home faucet of the elderly participants. All of the samples were transported to the Toxicology Laboratory of the Federal University of Amapa in a cold box within 1 hour of collection. Liquid specimens were refrigerated at 4 °C until processing.

Bacterial and fungal counts

The microbial quality, including the isolation and identification of pathogenic bacteria from commercial and homemade herbal medicines, was tested according to the regulations of the Brazilian Pharmacopoeia [16] and WHO standards [3]. The tests were used to quantify the number of bacteria and fungi isolated that are able to grow aerobically in 1 g or 1 mL of sample.

The samples were homogenized by mixing vigorously with or without previous maceration, of 1-g (semisolid or solid samples, soluble in water - when the product was water soluble or tween - when the product was fat soluble - 1% sample solution) or 1-mL (liquid samples) quantities of samples were transferred to 9 mL of casein-peptone (KASVI®). Then, serial dilutions were made to achieve an appropriate concentration. All microbial analyses were carried out in triplicate. Briefly, serial dilutions were made, and viability was assessed using the pour plate method on tryptic soy agar (KASVI®) or Sabouraud dextrose agar (KASVI®) for bacterial counts and fungal identification, respectively. All dehydrated media were prepared according to the manufacturer’s instructions and seeded and incubated at 37 °C for 2–5 days for bacterial screening and at 25 °C for 5–7 days for fungal screening [3,4,5,6,7,8,9,10,11,12,13,14,15,16]. At the end of the incubation period, the number of colony-forming units per gram (CFU/g) was calculated by multiplying the average number of colonies by the dilution factor. The obtained CFU/g of sample was compared with WHO standards [3]. Samples that presented bacterial growth greater than 105 CFU in 1 g of herbal medicine were considered unsatisfactory or inadequate according to WHO guidelines [3] for aerobic bacteria.

Identification of Bacteria

For bacterial isolation and identification, the samples were diluted in water or Tween, according to the solubility, and homogenized by vigorously mixing. The 1-mL aliquots were transferred to 9 mL of tryptone soy broth (KASVI®) or lactose broth (KASVI®) and cultured at the recommended time and temperature [16]. All microbial analyses were carried out in triplicate. For investigating Escherichia coli, Salmonella spp., Pseudomonas aeruginosa and Staphylococcus aureus, MacConkey agar (KASVI®), cetrimide agar (KASVI®), EMB agar (KASVI®), mannitol salt agar (KASVI®), Brilliant Green agar (KASVI®), and triple sugar iron agar (KASVI®) culture media were used. At the end of the incubation period, pathogenic bacterial isolates were preliminarily characterized by colony morphology, Gram staining, and biochemical tests (oxidase, gas and catalase production).

Water analysis

Detection of coliforms and E. coli in water samples was carried out in duplicate using Colilert® according to the manufacturer’s instructions and the techniques established by Standard Methods [17]. Yellow samples indicated the presence of coliform bacteria, and samples that were yellow and fluorescent when exposed to UV light (366 nm) indicated the presence of E. coli. Water samples were considered satisfactory or adequate, with an absence of total coliforms and/or E. coli in 100 mL, according to the Brazilian regulation for water quality for human consumption [18].

Statistical analyses

BioEstat® 5.3 software was used with bilateral hypotheses (μ1 ≠ μ0), 95% CI (confidence interval) and α = 0.05 (p ≤ 0.05) for performing statistical analyses. The descriptive statistics of sociodemographic variables (mean and standard deviation) are presented. Analysis of variance (ANOVA) and odds ratio were also used.

Results

Among the 132 herbal products analyzed, 83.3% were purchased from herbal shops or drugstores in different parts of the town of Macapa, while 16.7% were prepared from cultivated plants from a personal medicinal herb garden. Importantly, the samples include commercial/industrialized or technically elaborated product) or prepared by the elderly individuals themselves (homemade/herbalists). Of the study participants, 78.8% were women, with an average age of 69.4 ± 7.5 years. A total of 68.8% of the elderly participants were single, divorced or widowed, and 52.9% lived in suburban areas of the city. Approximately 23.1% of the participants were illiterate, and 50.5% had between 1 and 6 years of education. Regarding their monthly family income, 74% earned ≤588.80 dollars (Table 1).

Table 1 Demographic and socioeconomic characteristics of the elderly participants (N = 132)

The liquid herbal medicines analyzed included teas, tinctures, potions, syrups, and oils, and the semisolids were gels, creams, and balms. The solids included macerated plant parts or powdered plants, both of which were intended to be mixed in water or food (Table 2). Among herbal medicinal products, 68% were composed of several plants (6 ± 1.6), while only 22% of the homemade herbal medicines were prepared with a single plant species.

Table 2 Uses and characteristics of homemade herbal medicines and herbal medicinal products sold in different markets of Macapa, Brazil, from 2016 to 2017

Table 3 shows the ten most frequently reported herbal medicines used by elderly people along with their botanical names, reported properties and uses. Lippia alba (Mill.) N.E. Br (Cidreira) and Peumus boldus Molina (Boldo) were the most frequently consumed.

Table 3 Herbal medicines most frequently used by elderly people. Macapa, Brazil, from 2016 to 2017

For the evaluation of microbial contamination, the total number of viable bacterial and fungal colony-forming units per gram (CFU/g) were determined (Table 4). Among 132 samples of commercial and homemade herbal medicines, 51.5% had bacterial growth and 35.6% had observable fungal growth, independent of acceptable limits of contamination. A total of 31.8% of samples exceeded the safety limits (CFU/g ≤ 105) according to WHO guidelines [3] for aerobic bacteria, including 16.7% of the homemade herbal medicines and 15.1% of the commercial herbal medicines. It was also found that 23.5% of samples exceeded the safety limits for fungal growth. The liquid herbal medicine preparations administered orally were the most frequently contaminated. No statistically significant difference (p = 0.6313 / ANOVA) was found between the bacterial CFU/g (quantitative tests) found in homemade herbal medicines and that found in commercial herbal medicines. There was also no statistically significant difference (p = 0.5277 / ANOVA) between the fungal and bacterial CFU/g detected in the analyzed samples. When the differences in contamination between pathogenic bacteria (qualitative test) were significantly different (p = 0.005 / chi-square), it was demonstrated that the homemade herbal medicines had a higher risk of contamination by pathogenic bacteria than the commercial herbal medicines.

Table 4 Determination of the total viable bacterial and fungal counts (CFU/g) in herbal medicine samples

The microorganisms most commonly isolated from the homemade herbal medicines and commercial herbal medicine (Table 5) were S. aureus (49.2%), followed by Salmonella spp. (34.8%), E. coli (25.8%), and P. aeruginosa (14.4%). The results from the microbiological analyses of the homemade herbal medicines showed that S. aureus was isolated from 88.5% of the samples, Salmonella spp. were isolated from 69.2% of the samples, E. coli was isolated from 53.8% of the samples and P. aeruginosa was isolated from 25.0% of the samples. Among the commercial herbal medicines analyzed, 23.8% contained S. aureus, 12.5% contained Salmonella spp., and 7.5% contained E. coli and P. aeruginosa. The odds of identifying P. aeruginosa (odds ratio = 0.208, p = 0.001, 95% CI 114 ≤ μ ≥ 0.377) and E. coli (odds ratio = 0.429, p = 0.002, 95% CI 0.255 ≤ μ ≥ 0.721) were low. We also did not find any association between the odds of identifying S. aureus (odds ratio = 1.200, p = 0.537, 95% CI 0.739 ≤ μ ≥ 1.947) and the odds of identifying Salmonella spp. (odds ratio = 0.661, p = 0.131, 95% CI 0.403 ≤ μ ≥ 1.086).

Table 5 Pathogenic bacterial species isolated from herbal medicines consumed by elderly individuals

Table 6 presents the results for the identification of total coliforms and occurrence of E. coli in water samples used to prepare homemade herbal medicines. Of 18 samples analyzed, 14 (77.8%) had total coliforms, and E. coli was observed in 12 (66.7%), making them unfit for human consumption

Table 6 Total coliforms and E. coli detection in different water samples used to prepare homemade herbal medicines (N = 18)

Discussion

Herbal medicines are extensively used in Brazil due to the country’s diverse plant population, great sociodiversity, and conventional wisdom originating from three ethnic backgrounds (indigenous, African, and European) [21]. Presently, herbal medicines are used along with synthetic medicines to reduce health care costs for those individuals who have limited access to modern health care facilities [22] because these individuals do not have health insurance coverage and do not have much education [23]. Herbal medicines are inexpensive treatment options because they are easy to prepare or purchase in street markets that are common in the Amazon region.

Because of gradual devaluation of the knowledge associated with traditional health care-related practices [7], health surveys conducted in several countries have demonstrated greater use of herbal medicines as a mainstream practice among elderly people compared with that among young adults [8]. Regarding the sex of the elderly individuals studied, we observed that the majority of study participants were females, which can be justified by gender-based comparative studies on the knowledge of medicinal plants. These types of studies have demonstrated the social role of women (wives and daughters) in health care practices, including diagnosing illnesses, knowing prognoses, and being responsible for implementing the first treatments [2,3,4,5,6]. In a study of medicinal plants used by the local people of the Tafila area of Jordan, the traditional uses of these plants were investigated, and women were identified as the sole source of knowledge on herb use [24].

Among the herbal medicines most frequently used by the elderly population of the Brazilian Amazon, Lippia alba (Mill.) N.E. Br (Cidreira) and Peumus boldus Molina (Boldo) were the most common. These herbal medicines are consumed not only because of their therapeutic properties for the gastrointestinal tract [7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25] but also because of their calming and relaxing effects, which makes them multifunctional herbs. Generally, herbal medicines are used for treating simple diseases, such as digestive or respiratory diseases and general pain, whereas synthetic medicines are primarily used for blood pressure problems, general pain, and endocrine and nutritional diseases [26]. In studies that have included the Brazilian Atlantic Forest population, authors reported some species of medicinal plants that are commonly used in these regions, such as L. alba (Mill.) N.E. Br, Vernonia sp., C. citratus, P. boldus Molina, Matricaria chamomilla L, and Zingiber officinale [26].

The integration of plant-based medications into the primary health care system of developing countries is being expanded; however, safety issues continue to be neglected [1,2,3]. Bacterial and fungal contamination are frequent, especially in homemade herbal medicines, with CFU/g levels above recommended national [16] and international [3] standards. Herbal medicines in liquid pharmaceutical form for oral use presented the highest microbial contamination, and they were also the most consumed products among elderly people. Presumably, the proliferation of microorganisms may result from the failure to control moisture levels of herbal medicines during transportation and storage, as well as from the failure to control the temperatures of liquid forms and finished herbal products [3]. Moreover, most medicinal plants are prepared in an open environment in nonhygienic conditions that gradually lead to contamination with enteric pathogens with public health importance [26]. In the present study, of the 132 herbal medicine preparations, 31.8% were above the limit of acceptable bacterial counts according to WHO standards [3], indicating a risk in the consumption of the analyzed products. In other studies, bacterial counts were measured in herbal materials and herbal medicines [4,5,6, 14, 27,28,29], indicating risks in the consumption of these products.

Microbial analyses detected the presence of E. coli, Salmonella spp. and P. aeruginosa, which are all indications of fecal contamination, revealing poor hygiene conditions in the preparation and storage of these herbal medicines. The presence of bile-tolerant gram-negative bacteria belonging to the family Enterobacteriaceae is an important indicator of hygienic precariousness, inadequate processing or postprocessing contamination. Pathogens of this family are potential causative agents of foodborne diseases, increasing the risk for consumers to develop intestinal tract infections [30]. Since the detection of E. coli is indicative of fecal contamination, it can be concluded that the herbal medicines that contained this microorganism were contaminated directly or indirectly by human or animal feces and were therefore unsuitable for consumption [31].

The analyses of this study also detected the presence of S. aureus, which can cause staphylococcal gastroenteritis, scalded-skin syndrome, and folliculitis, among other diseases [31]. A study that also evaluated the microbial quality of herbal medicines showed similar results, with 47.6% of samples contaminated with E. coli, 33% of samples contaminated with Salmonella spp., and 71.4% of samples contaminated with S. aureus [32]. Pathogenic bacteria, such as E. coli, Salmonella spp., Shigella, S. aureus and P. aeruginosa, were also found in other studies [30, 31]. These contaminations were probably caused by unsafe collection, transportation, drying, preparation, storage or dispensing processes of the herbal medicines [30].

The quality of the water used in the preparation of herbal medicines may have contributed to the high level of bacterial contamination observed for the homemade herbal medicines. Drinking water should be free from pathogenic microorganisms and bacteria that indicate fecal contamination [33]. However, 66.7% of the water samples used for the preparation of herbal medicines were not adequate for consumption. The problem may be related to the lack of basic sanitation and the inadequate management of human and animal dejections incorporated into the soil, which are the most important factors in the contamination of water resources [34]. The water quality and notions of hygiene are likely related to the differences in the contamination of pathogenic bacteria in the herbal medicines and herbal medicine products identified in this study.

Characterization of fungal colonies, although not required by the Brazilian Pharmacopoeia [16], is important in assessing the risk of analyzed products. Microscopic analysis suggested fungal contamination that was similar to another study that demonstrated the presence of fungal species known to be able to produce mycotoxins, such as Aspergillus niger, Aspergillus ochraceus, Aspergillus flavus and Aspergillus parasiticus [35]. These species may pose a risk when present in products used orally. Many studies have also demonstrated the presence of mycotoxins in preparations derived from medicinal plants [34]. The severity of mycotoxins depends on the toxicity, degree of exposure, age and nutritional status of the individual and the possible synergistic effects of other chemical agents to which they are exposed [36].

Good manufacturing practices in pharmacies or industries that handle herbal medicines are essential. Beyond compliance, following current national and international legislations, such as European Scientific Cooperative on Phytotherapy and Brazilian Pharmacopoeia, is important [3, 16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38]. It is also essential to monitor establishments that market herbal medicines by checking that they have a license from the health authority for this trade and that the products are registered and authorized for consumption [39], as cases of falsification or commercialization of irregular herbal medicines may occur.

In search of solutions for the irrational use of herbal medicines, programs were created to provide standards for the correct use of medicinal plants and select them according to their efficacy and safety, replacing the routine empirical use carried out by communities [40,41,42]. These initiatives, however, were not sufficient to guarantee the triad of efficacy, safety, and quality of the products used in herbal medicine, resulting in the marketing and consumption of products that do not meet the minimum criteria of microbial quality standards [3]. Other countries that culturally use herbal medicines [5, 7, 14, 22, 27, 41, 42] have also faced issues of quality incompliance in herbal medicines because of the presence of pathogenic bacteria. This dynamic shows that quality standards and product safety criteria have not yet been achieved in this complementary medical practice, which probably results in reduced teaching on herbal medicines in medical schools.

Pharmacovigilance of medicinal plants is also important and requires the collection of more information on the methods of preparation and administration, adverse events, contraindications and precautions for a better risk-effectiveness ratio [43]. The need for more effective monitoring of the commercialization and consumption of herbal medicines by elderly individuals has become evident because the risks are real and significant. Strategies for health education, campaigns and workshops for elderly people on the safe use of these therapies are essential for public health and patient safety.

Conclusions

This study demonstrated the presence of aerobic bacteria and fungi above the acceptable limits as well as the presence of pathogenic bacteria in samples of herbal medicines used by elderly individuals in the Brazilian Amazon region. These findings demonstrate important risks for elderly individuals associated with the use of herbal medicines and the need for surveillance and the establishment of stricter control procedures in the production/preparation and marketing of these herbal medicines to guarantee quality. These steps will help to avoid additional risks to the elderly population of the city of Macapa in the consumption of herbal medicines, which is a common cultural health care habit in this Brazilian region. Control programs for the sale of these herbal medicines should be implemented by national regulatory agencies to prevent or reduce the consumption of products outside the minimum standards of quality. In addition, campaigns linked to primary health care units or family health programs with the aim of guiding the proper preparation of herbal medicines (avoiding microbial contamination) should be initiated in the region.

Availability of data and materials

All available data can be obtained from the corresponding author. All data will be shared in a way that safeguards the confidentiality and anonymity of the study participants.

Abbreviations

CFU/g:

Forming Units Colonies for 1 g

CI:

(Confidence Interval)

WHO:

World Health Organization

References

  1. World Health Organization, WHO. Traditional Medicine Strategy 2002–2005 2002. Geneva, Switzerland.

  2. Umair M, Altaf M, Abbasi AM. An ethnobotanical survey of indigenous medicinal plants in Hafizabad district, PunjabPakistan. PLOS ONE 2017;2. doi.org/10.1371/journal.pone.0177912.

  3. World Health Organization, WHO. WHO guidelines for assessing quality of herbal medicines with reference to contaminants and residues 2007. Press, Geneva, Switzerland.

  4. Kosalec I, Cvek J, Tomic S. Contaminants of medicinal herbs and herbal products. Arch Ind Hyg Toxicol. 2009;60(4):485–501.

    CAS  Google Scholar 

  5. Danladi A, Inabo I, Yakubu E, Olonitola S. Contamination of herbal medicinal products marketed in Kaduna metropolis with selected pathogenic bacteria. Afr J Tradit Complement Altern Med. 2009;6(1):70–7.

    Google Scholar 

  6. Khattak F. Microbiological quality assessment of commercially available medicinal plants in Peshawar city, Pakistan. Pak J Bot. 2012;44(4):1203–8.

    Google Scholar 

  7. Medeiros PM, Ladio AH, Alburqueque UP. Patterns of medicinal plant use by inhabitants of Brazilian urban and rural areas: a macroscale investigation based an available literature. J Ethnopharmacol. 2013;150:729–49.

    Article  Google Scholar 

  8. Bardia A, Nisly NL, Zimmerman MB, Gryzlak BM, Wallace RB. Use of herbs among adults based on evidence-based indications: findings from the National Health. Interview Survey Clin Proc. 2007;82:561–6.

    Article  Google Scholar 

  9. World Health Organization, WHO. The world health report 2002 - Reducing risks, promoting healthy Life 2002. Press, Geneva, Switzerland.

  10. Almeida ST, Valentim AL, Diefenbach N. Lian Gong como prática fisioterápica preventiva do envelhecimento. Estudos interdisciplinares do Envelhecimento. 2004;6(1):103–10.

    Google Scholar 

  11. Civinski C, Montibeller A, Braz ALO. A Importância do exercício físico no envelhecimento. Revista da Unifebe. 2011;9(1):163–75.

    Google Scholar 

  12. Mann HJ, Steiner JF, Willett MS. Drug use in the elderly: A position statement of the American College of clinical pharmacy. Pharmacotherapy, 1988. doi.org/10.1002/j.1875-9114.1988.tb04094.x.

  13. Souza PM, Souza LL, Silveira CAN. Fármacos em idosos. In: Formulário Terapêutico Nacional 2008. Brasília: Ministério da Saúde; 2008. p. 26–29p.

    Google Scholar 

  14. Famewo EB, Clarke AM, Afolayan AJ. Identification of bacterial contaminants in polyherbal medicines used for the treatment of tuberculosis in Amatole District of the Eastern Cape Province, South Africa, using rapid 16S rRNA technique. J Health Popul Nutr. 2016;35(1):27.

    Article  Google Scholar 

  15. Instituto brasileiro de geografia e estatística [https:www.ibge.gov.br]. Análise do panorama das cidades brasileiras. Dados populacionais de Macapá []. Available from: http:www.ibge.gov.br. (In Portuguese).

  16. Agência Nacional de Vigilância Sanitária - ANVISA [Brazil]. Farmacopeia Brasileira. Brasília: Anvisa, 2010. 5th ed Vol 1; p.546. (In Portuguese).

  17. Rice EW, Baird R, Eaton AD, Clesceri LS. Standard Methods for the Examination of Water. American Public Health Association, American Water Works Association, Water Environment Federation 2012:22nd ISBN: 978–087553-0130.

  18. Agência Nacional de Vigilância Sanitária [Brazil]. PORTARIA N° 2.914, DE 12 de dezembro de 2011.Dispõe sobre os procedimentos de controle e de vigilância da qualidade da água para consumo humano e seu padrão de potabilidade.. Diário Oficial da União: Jan 2012; (In Portuguese).

  19. Banco Central do Brasil [www.bcb.gov.br]. Câmbio e capitais internacionais. Taxas de câmbio. Dólar americano. []. Available from: http: www.bcb.gov.br. (In Portuguese).

  20. THE PLANTS LIST®database [www.theplantlist.org/]. The Plant List is a working list of all known plant species. []. Available at: http: www.theplantlist.org.

  21. Ribeiro AQ, Leite JPV, Dantas-Barros AM. Profile of phytotherapeuticals usage in community drug stores in Belo Horinzonte city under national legislation. Brazilian Journal of Pharmacognosy. 2005;15(1):65–70.

    Article  Google Scholar 

  22. Kebede D, Alemayehu A, Binyam G, Yunis M. A historical overview of traditional medicine practices and policy in Ethiopia. Ethiop J Health Dev. 2006;20(2):127–34.

    Google Scholar 

  23. Delgoda R, Younger N, Barrett C, Braithwaite J, Davis D. The prevalence of herbs use in conjunction with conventional medicines in Jamaica. Complementary therapies in medicine. 2010;18(1):13–20. https://doi.org/10.1016/j.ctim.2010.01.002.

    Article  PubMed  Google Scholar 

  24. Abdelhalim A, Aburjai T, Hanrahan J, Abdel-Halim H. Medicinal Plants Used by Traditional Healers in Jordan, the Tafila Region. Pharmacogn Mag. 2017;13(Suppl 1):S95–S101. https://doi.org/10.4103/0973-1296.203975.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Badke MR, Budó MLD, Alvim NAT, Zanetti GD, Heisler EV. Saberes e práticas populares de cuidado em saúde com o uso de plantas medicinais. Contexto Enferm. 2012;21(2):363–70 (In Portuguese).

    Article  Google Scholar 

  26. Zank S, Hanazaki N. The coexistence of traditional medicine and biomedicine: A study with local health experts in two Brazilian regions. PLoS One. 2017;12(4):e0174731 doi.org/10.1371/journal.pone.0174731.

    Article  Google Scholar 

  27. Govender S, Du Plessis-Stoman D, Downing TG, Van de Venter M. Traditional herbal medicines: microbial contamination, consumer safety and the need for standards. S Afr J Sei. 2006;102(5):253–5.

    Google Scholar 

  28. Kneifel W, Czech E, Kopp B. Microbial contamination of medicinal plants. Planta Med. 2002;68:5–15 https://doi.org/10.1055/s-2002-20060.

    Article  CAS  Google Scholar 

  29. Yesuf A, Wondimeneh Y, Gebrecherkos T, Moges F. Occurrence of Potential Bacterial Pathogens and Their Antimicrobial Susceptibility Patterns Isolated from Herbal Medicinal Products Sold in Different Markets of Gondar Town, Northwest Ethiopia. International Journal of Bacteriology. 2016;11:ID 1959418.

    Google Scholar 

  30. Trabulsi LB, Alterthum F. Microbiologia. 6th ed. Atheneu, 2015. (In Portuguese).

  31. Esimone CO, Oleghe PO, Ibezim EC, Okeh CO, Iroha IR. Susceptibility-resistance profile of micro-organisms isolated fromherbal medicine products sold in Nigeria. Afr J Biotechnol. 2007;6(24):2766–75.

    Article  CAS  Google Scholar 

  32. Kaume L, Foote JC, Gbur EE. Microbiologiacal contamination of herbs marketed to HIV-infected people in Nairobi (Kenya). S Afr J Sci. 2012;108(9):80–3.

    Google Scholar 

  33. Mattos MLT, Silva MD. Controle da qualidade microbiológica das águas de consumo na microbacia hidrográfica Arroio Passo do Pilão. Ministério da Agricultura, Pecuária e Abastdo Pilão. Ministério da Agricultura, Pecuária e Abastecimento, comunicado técnico 2002;61.

  34. Bugno A, Buzzo AA, Nakamura CT, Pereira TC, Matos D, Pinto TJA. Avaliação da contaminação microbiana em drogas vegetais. Revista Brasileira de Ciências Farmacêuticas. 2005;41:4.

    Article  Google Scholar 

  35. Candlish AAG, Pearson SM, Aidoo KE, Smith JE, Kelly B, Irvine H. A survey of ethnic foods for microbial quality and aflatoxin content. Food Addit Contam. 2001;18(2):129–36 https://doi.org/10.1080/02652030010021404.

    Article  CAS  Google Scholar 

  36. Maziero MT, Bersot LS. Micotoxinas em alimentos produzidos no Brasil. Revista Brasileira de Produtos Agroindustriais. 2010;12(1):89–99.

    Article  Google Scholar 

  37. Bettega JMPR, Machado MR, Presibella M, Baniski G, Barbosa CA. Métodos analíticos no controle microbiológico de agua para consumo humano. Cienc. agrotec. [online]; 2006; 30(5):950–954.

    Article  Google Scholar 

  38. Matos FJ. A. Farmácia Vivas. 3rd ed. Fortaleza: UFC 1998. p.179. (In Portuguese).

  39. Ministério da Saúde (Brasil). Portaria n°. 886, de 20 de abril de 2010. Institui a Farmácia Viva no âmbito do Sistema Único de Saúde (SUS). Diário Oficial da União 22 abril 2010; Seção 1. (In Portuguese).

  40. Agência Nacional de Vigilância Sanitária [Brazil]. Resolução da Diretoria Colegiada n°18, de 03 de abril de 2013. Dispõe sobre as boas práticas de processamento e armazenamento de plantas medicinais, preparação e dispensação de produtos magistrais e oficinais de plantas medicinais e fitoterápicos em farmácias vivas no âmbito do Sistema Único de Saúde (SUS). Diário Oficial da União:16 mar 2000; Seção1. (In Portuguese).

  41. Ogunshe AAO, Kolajo TT. In vitro phenotypic antibiotic resistance in bacterial flora of some indigenous orally consumed herbal medications in Nigeria. Journal of Rural and Tropical Public Health. 2006;5:9–15.

    Google Scholar 

  42. Adeleye IA, Okogi G, Ojo EO. Microbial contamination of herbal preparations in Lagos, Nigeria. J Health Popul Nutr. 2005;23(3):296–7.

    CAS  PubMed  Google Scholar 

  43. Mastroianni PC, Luchetta RC. Regulamentação Sanitária de Medicamentos. Rev Ciênc Farm Básica Apl. 2011;32(1):127–32 (In Portuguese).

    Google Scholar 

Download references

Funding

No funding was obtained for this study.

Author information

Authors and Affiliations

Authors

Contributions

CMSL: participated in all stages of the work. MATF: design and conception of the research work; analysis and interpretation of data; statistical analysis; critical review of the manuscript. BPL: data collection; analysis and interpretation of data. PCM: research design; critical review of the manuscript. FFOS: conception and design of the research. JOS: data analysis and interpretation; writing of the manuscript; critical review of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Carolina Miranda de Sousa Lima.

Ethics declarations

Ethics approval and consent to participate

The work described has been carried out under The Code of Ethics of the World Medical Association (Declaration of Helsinki) for experiments involving humans. This project was approved by the Ethics Committee on Human Research of the Federal University of Amapa with authorization no. 38400314.9.0000.0003. The evaluation of the elderly was carried out only after all parties signed the Free and Informed Consent Terms (FICT). All participants of the study provided written informed consent.

Consent for publication

Not applicable because to no include any individual person’s data in any form (including individual details, images or videos).

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Sousa Lima, C.M., Fujishima, M.A.T., de Paula Lima, B. et al. Microbial contamination in herbal medicines: a serious health hazard to elderly consumers. BMC Complement Med Ther 20, 17 (2020). https://doi.org/10.1186/s12906-019-2723-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12906-019-2723-1

Keywords