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PLOS One logoLink to PLOS One
. 2021 Jul 1;16(7):e0253971. doi: 10.1371/journal.pone.0253971

Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia

Demelash Demissie 1, Teshome Geremew 1, Adinew Zewdu Chernet 2, Musa Mohammed Ali 3,*
Editor: Praveen Rishi4
PMCID: PMC8248621  PMID: 34197544

Abstract

Introduction

Antibiotics are commonly used for the treatment and prevention of bacterial infections. The potency of antibiotics can be affected by factors such as temperature, light, moisture, and storage conditions. Inappropriate storage and transportation of antibiotics may lead to loss of potency earlier than the expiry date. The aim of this study was to determine the potency and associated factors of commonly retailed antibiotics.

Method

Institution-based cross-sectional study was conducted on commonly retailed antibiotics in pharmacies that are available in Adama, Ethiopia from March 2018 to June 2018. This study focused on commonly ordered antibiotics such as amoxicillin, azithromycin, ciprofloxacin, and ceftriaxone. Antibiotics to be tested were selected by using a simple random sampling technique. Socio-demographic and related data were collected using a semi-structured questionnaire. Antibiotic susceptibility testing was performed using the disc diffusion method as described in the Clinical Laboratory Standard Institute guideline.

Results

Mean inhibition zones of amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone were 14.2 ± 4 mm, 30.9 ± 4.2 mm, 17.47 ± 3.83 mm, and 32.7±1.8 respectively. Out of 164 antibiotics tested, 61% passed the potency test. The potency of antibiotics varies across different countries in which 53.7% and 54.6 of antibiotics from India and Ethiopia passed the potency test. All ceftriaxone tested in this study passed the potency test. Factors such as air condition of pharmacy (X2 = 4.27; p = 0.039), source of all antibiotics (X2 = 5.41; p = 0.02), and source of amoxicillin (X2 = 4.73; p = 0.03) were significantly associated with potency of antibiotics.

Conclusions

About 40% of antibiotics tested in the current study did not pass the potency test; this warrants further investigation to identify the magnitude of the problem and its causes at a large scale.

Introduction

Antibiotics have been used for the treatment and prevention of bacterial infections [1]. The effectiveness of antibiotics can be affected by temperature, light, moisture, and storage condition [2]. Counterfeit and substandard antibiotics can also affect the quality of antibiotics. Counterfeit antibiotics are deliberately mislabeled with a fake identity, composition, and source. This can affect generic and branded antibiotics and may include wrong ingredients, no active pharmaceutical ingredients (APIs), and insufficient ingredients. And it also includes antibiotics which are sold with fake labeling and fake packaging [3].

Substandard antibiotics are produced by manufacturers authorized by the national medicine regulatory authority which does not meet the specifications set by national standards [4]. A mild difference in the concentration of the active ingredient during antibiotic preparation may cause allergic reactions, unexpected side effects, poisoning, untreated disease, and early death [5,6]. Careful in vitro evaluations are necessary at regular intervals to check the potency of antibiotics sold in the pharmacies [7].

Despite the role of antibiotics in treating the disease; ineffective antibiotics can pose great risks to individuals and even threaten the lives of consumers [8]. Degradation of antibiotics occurs much before they approach the expiry dates because of several factors such as exposure to light and moisture [9]. The loss of potency during storage may influence the efficacy and safety of antibiotics [10].

Poor-quality antibiotics can reach the market through substandard production of legitimate antibiotics due to inadequate quality-control processes during manufacturing, as well as by deliberate fraudulent practices [11]. The wide use of antibiotics with poor quality can lead to the emergence and spread of antibiotic-resistant strains of bacteria in the community [12]. Infection caused by antibiotic-resistant bacteria are more difficult to treat, can lead to long-term illness, increase healthcare costs, and death [9].

Expansion of pharmaceutical industries in many countries with advancement in transportation technologies facilitated not only trade of genuine pharmaceutical products but also the circulation of poor-quality and counterfeited antibiotics in list-income countries [13]. Adama is situated along the road that connects Addis Ababa with Dire-Dawa city. A large number of trucks use the same route to travel to and from the seaports of Djibouti and additionally, the new Addis Ababa-Djibouti railway runs through Adama. This makes Adam one of the busiest cities in the country with strong business activities and several kinds of illegal commodities including counterfeit antibiotics that might be sold in pharmacies found in Adama city. The aim of this study was to determine the potency and associated factors of commonly sold antibiotics in pharmacies that are found in Adama city.

Materials and methods

Study setting

This study was conducted in pharmacies located in Adama, Oromia Regional State, Ethiopia. Adama is situated at 99 km to the southeast of Addis Ababa at an altitude of 1712 meters above sea level between the base of an escarpment to the west, and the Great Rift Valley to the East.

Study design and study population

An institution-based cross-sectional study was conducted on commonly retailed antibiotics from March 2018 to June 2018. In this study, all pharmacies in Adama were included. A total of 164 antibiotics belonging to four categories of antibiotics were included. These antibiotics were amoxicillin (n = 42), ciprofloxacin (n = 42), azithromycin (n = 38), and ceftriaxone (n = 42). From each pharmacy, one antibiotic was randomly selected. Four pharmacies did not have azithromycin. Antibiotics were selected because they are commonly ordered in the study area. Amoxicillin was in the form of a capsule (one stripe contains 10 capsules); ciprofloxacin was in the form of tablets (one stripe contains 10 tablets), and azithromycin was in the form of tablet (one stripe contains 3 tablets). Ceftriaxone was in the form of vials.

Recommended storage condition of evaluated antibiotics

During the study period, all antibiotics tested in this study were stored in a room with good ventilation and a temperature range of 2–30°C.

Study variables

Dependent variable: Potency of antibiotics.

Independent variables: Type of pharmacy, air condition of pharmacy, the shelf life of antibiotics, and source of antibiotics.

Data collection

We developed a semi-structured questionnaire to collect socio-demographic characteristics of dispensers and the condition of antibiotics and pharmacies. From each pharmacy, one pharmacist or druggist was interviewed. All selected antibiotics were checked for batch numbers, manufacturer, and expiry date. After the assessment, antibiotics were transported to the Oromia Public Health Laboratory (OPHL) for antimicrobial susceptibility testing.

Antibiotic disc preparation

To prepare antibiotic disc we followed the procedure suggested by Clinical Laboratory Standard Institute (CLSI) [14]. Discs with 6 mm diameter were prepared by punching a sheet of Whatman Number 3 filter paper (United Kingdom) using a perforator. To obtain 10 μg of amoxicillin disc, 500 mg of amoxicillin tablet was dissolved in 250 ml of phosphate buffer and 5 μL of dissolved stock antibiotic was impregnated onto the 6 mm sized disc. To obtain 5 μg of ciprofloxacin disc, 500 mg of ciprofloxacin tablet was dissolved in 500 ml of distilled water and 5 μL of dissolved stock antibiotic was impregnated onto the 6 mm sized disc. To obtain 30 μg of ceftriaxone, 1000 mg of injectable ceftriaxone was dissolved in 166.7 ml of distilled water and 5 μL of dissolved stock antibiotic was impregnated onto the 6 mm sized disc. To obtain 15 μg of azithromycin, 500 mg of azithromycin tablet was dissolved in a 166.7 ml of 95% ethanol with a broth media and 5 μL of dissolved stock antibiotic was impregnated onto the 6 mm sized disc (S1 Table in S1 File). To assess the potency of antibiotics, two reference strains such as Escherichia coli (ATCC-25922) and Staphylococcus aureus (ATCC-25923) were used.

Antimicrobial susceptibility testing

The antimicrobial susceptibility testing was performed following the Kirby-Bauer disc diffusion method as described in the CLSI [14]. Briefly, the reference strains (E. coli and S. aureus) were sub-cultured onto blood agar and incubated at 37°C overnight. Using a sterile wire loop, 3–5 pure colonies were emulsified in 5 mL of normal saline until the turbidity matches 0.5 McFarland standard. Using a sterile dry cotton swab, bacterial suspensions were uniformly inoculated onto the entire surface of Muller Hinton agar (MHA). Antibiotics disks were placed on the surface of MHA and incubated aerobically at 37°C for 16–18 hours. The diameter of the zone of inhibition was measured using a ruler; isolates were classified as potent (pass) or not potent (fail) based on the CLSI cut point [14]. All experiments were conducted in triplicates and the means were recorded to determine the potency of antibiotics.

Pass criteria based on the susceptibility range set by CLSI

Amoxicillin: It is considered as ‘pass’ if the diameter of the zone of inhibition falls within or greater than the susceptibility range of 15–22 mm.

Ciprofloxacin: It is considered as ‘pass’ if the diameter of the zone of inhibition falls within or greater than the susceptibility range of 30–40 mm.

Azithromycin: It is considered as ‘pass’ if the diameter of the zone of inhibition falls within or greater than the susceptibility range of 21–26 mm.

Ceftriaxone: It is considered as ‘pass’ if the diameter of the zone of inhibition falls within or greater than the susceptibility range of 29–35 mm.

Data quality control

The semi-questionnaire was validated and pretested before use in the actual study. All laboratory tests were performed according to the CLSI guideline. The sterility and performance of the culture media were checked; the performances of all reagents and materials were checked and ensured. Prior to use, all discs were sterilized and the sterility was checked by placing 8 randomly selected discs on uninoculated MHA agar and incubated at 37°C for 18 hours. Selected discs impregnated with only solvent were checked for antibacterial activity. The disc diffusion method used in the current study was verified by running the method 20 times using standard antibiotics obtained from OPH: Amoxicillin (10 μg), ciprofloxacin (5 μg), azithromycin (15 μg), and ceftriaxone (30 μg). The precisions for amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone were 2.364 mm, 3.364 mm, 1.63 mm, and 1.67 mm respectively. The uncertainty measurement for amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone with a 95% CI were 17–19 mm, 31–32 mm, 21–24 mm, and 31–33 mm respectively.

Data management and analysis

Data were checked, coded, and entered into the computer using EP INFO version 7 and analyzed by using a Statistical Package for Social Sciences (SPSS) version 20. Data were analyzed using Chi-square (X2); a p-value of < 0.05 was considered as statistically significant.

Results

Socio-demographic data

In this study, a total of 42 pharmacies were included. Out of which, 81% belongs to the private and 19% belongs to the government. A total of 42 dispensers (13 males and 29 females) were interviewed. The ages of 45.2% of dispensers were between 31–40 years. The work experience of 54.8% of dispensers was 5–9 years (Table 1).

Table 1. Characteristics of dispensers and types of Pharmacy at Adama, Oromia, Ethiopia, March 2018 to June 2018 (N = 42).

Variables Category n (%)
Type of Pharmacy Private 34 (81)
Government 8 (19)
Sex of dispensers Male 13 (31)
Female 29 (69)
Age of dispensers in years ≤25 4 (9.5)
26–30 15 (35.7)
31–40 19 (45.2)
41–49 4 (9.5)
≥50 -
Qualification of dispensers Druggist 8 (19)
Pharmacist 34 (81)
Work experience of dispensers in years <1 -
1–4 6 (14.3)
5–9 23 (54.8)
10–14 9 (21.4)
≥15 4 (9.5)

Characteristics and source of antibiotics

Most amoxicillin was manufactured in Ethiopia (73.8%) whereas most ciprofloxacin was manufactured in South Korea and Romania. Most of the ceftriaxone were manufactured in China (Table 2).

Table 2. Frequency of antibiotics based on manufacturers at Adama, Ethiopia, March 2018 to June 2018.
Antibiotics Manufacturer n (%)
Amoxicillin APF (Ethiopia) 15 (35.7)
DENK-Pharma (Germany) 1 (2.4)
EPHARM (Ethiopia) 16 (38.1)
GlaxoSmithKline (UK) 3 (7.1)
Kopra Ltd (India) 6 (14.3)
Remedica (Cyprus) 1 (2.4)
Total 42 (100)
Ciprofloxacin APF (Ethiopia) 4 (9.5)
Brawn Lab (India) 1 (2.4)
Cadila Pharmaceutical (Ethiopia) 4 (9.5)
EPHARM(Ethiopia) 6 (14.3)
Huonsco Ltd (S. Korea) 10 (23.8)
Leben laboratories (India) 7 (16.7)
Sandoz a Navartis Company (Romania) 10 (23.8)
Total 42 (100)
Azithromycin Bafna Pharmaceutical Ltd (India) 1 (2.6)
Beximco pharmaceutical Ltd (Bangladesh) 7 (18.4)
Cadila Pharmaceuticals (Ethiopia) 9 (23.7)
Coral Laboratories Ltd (India) 2 (5.3)
Corporation Ltd (Kenya) 1 (2.6)
Deva Holding (Turkey) 5 (13.2)
EPHARM (Ethiopia) 1 (2.6)
Sandoz a Navartis company (Romania) 2 (5.3)
Sherya life science (India) 1 (2.6)
Umedica Laboratories Ltd (India) 1 (2.6)
ZIM Laboratories Ltd (India) 8 (21.1)
Total 38 (100)
Ceftriaxone Ashish Life Science (India) 6 (14.3)
AsralSteriTech PLC Ltd (India) 5 (11.9)
BilimPharmaceutical (Turkey) 2 (4.8)
CSPC ZhougnuoPharm (China) 9 (21.4)
Gulf Pharmaceuticalind (UAE) 3 (7.1)
Shandonglukang pharmaceutical (China) 13 (30.9)
Theon Pharmaceutical (India) 2 (4.8)
VHB medi science ltd (India) 1 (2.4)
Zhuhai Kinhoo pharmaceutical (China) 1 (2.4)
Total 42 (100)

EPHARM: Ethiopian pharmaceutical manufacturing, APF: Addis pharmaceutical factory plc (private limited company), UAE: United Arab Emirates, UK: United Kingdom.

Shelf life and handling conditions of antibiotics

Almost all antibiotics retailed in the private and government pharmacies in Adama had a long expiry date (> six months). At the time of collection, none of the antibiotics were expired. All amoxicillin and ciprofloxacin had a long expiry date. Thirty (78.9%) and 38 (90.5) azithromycin and ceftriaxone had a long expiry date respectively. Forty (90.5%) of the pharmacies had enough storage area. Out of 42 pharmacies, 25 (59.5%) had ventilator with good working conditions, 32 (76.2%) had refrigerator and 26 (61.9%), and 25 (59.5%) of them had a thermometer in dispenser and store room respectively. Thirty-eight (90.5%) of the respondents replied that there was an inspection by a regulatory body. Thirty-one (81.6%) of respondents replied that inspection was made in three months intervals and 7 (18.4%) replied that inspection was made in six months intervals.

Mean inhibition zones of antibiotics

Mean inhibition zones of amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone were 14.2 ± 4 mm, 30.9 ± 4.2 mm, 17.47 ± 3.83 mm, and 32.7±1.8 respectively. Most of the amoxicillin from Ethiopia (EPHARM-Ethiopia) had a mean zone of inhibition of less than 12 mm (Table 3).

Table 3. Mean zone of inhibition of selected antibiotics collected from pharmacies found in Adama, Ethiopia, March 2018 to June 2018.

Bacteria Amoxicillin manufacture n Mean ZI (mm±SD) Standard range(mm)
E. coli (E. coli ATCC 25922) APF-Ethiopia 15 14.73±3.4 15–22
DENK Pharma-Germany 1 15 ±0
EPHARM-Ethiopia 16 11.88±4.7
GSK-London 3 14.67± 3.2
KOPRA LIMTED-India 6 21.33±2.3
Remedica-Cyprus 1 15±0
Mean IZ of Amoxicillin 42 14.2±4.0
Ciprofloxacin manufacturer and country
E. coli (ATCC 25922) APF-Ethiopia 4 34±7.1 30–40
BRAWN Lab.-India 1 32±0
CADILA Pharmaceutical- Ethiopia 4 34±2.8
EPHARM-Ethiopia 6 32.5±4.6
Huonsco Ltd- S. korea 10 31.1±1.9
Leben lab.-India 7 26.3±8.2
SANDOZ aNavartis-Romania 10 29.1±3.5
Mean IZ of ciprofloxacin 42 30.9±4.2
Azithromycin manufacture and country
S. aureus (ATCC 25923) Bafna Pharmaceutical-India 1 12±0 21–26
Beximico pharmaceutical -Bangladesh 7 16.5±4.57
CADILA Pharmaceutical -Ethiopia 9 18.5±3.5
Coral Lab.-India 2 19.33±4.18
Corporation limited-Kenya 1 20±0
Deva Holding-Turkey 5 19.33±4.18
EPHARM-Ethiopia 1 14±0
Sandoz–Romania 2 17±4.2
SHERYA LIFE Science- India 1 20±0
Umedica Laboratory-India 1 14±0
ZIM lab.-India 8 16.12±3.5
Mean ZI of Azithromycin 38 17.47±3.83
Ceftriaxone manufacturer and country
E. coli (ATCC 25922) Ashish life science-India 6 33±1.7 29–35
Asralsteril Tech-India 5 32.4±1.3
BILIM pharmaceutical- Turkey 2 34±1.4
CSPC Zhougnuo Pharmaceutical-China 9 33.2±1.4
Gulf pharmaceutical industry-UAE 3 32±1.7
Shandonglukang pharmaceutical-China 13 32.5±3
Theon Pharmaceutical-India 2 32±1.4
VHB MEDI Science limited-India 1 35±0
Zhuhai Kinhoo pharmaceutical- China 1 33±0
Mean IZ of ceftriaxone 42 32.7±1.8

Mm: millimeter, SD: Standard deviation, ZI: Zone of inhibition, ATCC: American type culture collection, UAE: United Arab Emirates.

Potency of antibiotics

Out of 164 antibiotics tested in this study, 61% were potent. 53.7% and 54.6 of antibiotics from India and Ethiopia were potent respectively (Table 4). The total potency of amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone were 50%, 66.7%, 23.7%, and 100% respectively (Table 5).

Table 4. Potency of selected antibiotics collected from pharmacies found in Adama, Ethiopia based on the source country, March 2018 to June 2018.

Country Pass n (%) Fail, n (%) Total
India 22 (53.7) 19 (46.3) 41
Bangladesh - 7 (100) 7
Ethiopia 30 (54.6) 25 (45.5) 55
Kenya - 1 (100) 1
Turkey 6 (85.7) 1(14.3) 7
Romania 3 (25) 9 (75) 12
Germany 1 (100) - 1
United Kingdom 2 (66.7) 1 (33.3) 3
Cyprus 1 (100) - 1
S. Korea 9 (90) 1 (10) 10
China 23 (100) - 23
UAE 3 (100) - 3
Total 100 (61) 64 (39) 164

UAE: United Arab Emirates, S. Korea: South Korea.

Table 5. Potency of selected antibiotics collected from pharmacies found in Adama, Ethiopia based on the manufacturer and country, March 2018 to June 2018.

Amoxicillin
Manufacturer Country Brand name Concentration Pass, n (%) Fail, n (%) Total
APF Ethiopia Amoxid 500mg 6(40) 9 (60) 15
DENK Pharma Germany Amoxi-Denk 500mg 1 (100) - 1
EPHARM Ethiopia Amoxicillin 500mg 8 (50) 8 (50) 16
GlaxoSmithKline UK Amoxil 500mg 2 (66.7) 1 (33.3) 3
KOPRA limited India AMYN 500mg 3 (50) 3(50) 6
Remedica Cyprus Amoxapen 500mg 1 (100) - 1
Total 21 (50) 21 (50) 42
Ciprofloxacin
APF Ethiopia CIF LOX 500mg 3 (75) 1 (25) 4
BRAWN Laboratory India Brucipro 500mg 1 (100) - 1
CADILA Pharmaceutical Ethiopia Ciprodac 500mg 4 (100) - 4
EPHARM Ethiopia Ciprofloxacin 500mg 5 (88.3) 1 (16.7) 6
Huonsco Ltd S. Korea Floxine 500mg 9 (90) 1 (10) 10
Leben laboratory India Ciproleb 500mg 3 (42.9) 4 (57.1) 7
SANDOZ aNavartis comp Romania Serviflox 500mg 3 (30) 7 (70) 10
Total 28 (66.7) 14 (33,3) 42
Azithromycin
Bafna Pharmaceutical India AZIBIAL 500mg - 1 (100) 1
Beximico pharmaceutical Bangladesh Azithrocin 500mg - 7(100%) 7
CADILA Pharmaceutical Ethiopia Zycin 500mg 4 (44.4) 5 (55.6) 9
Coral Laboratory India Cortzite 500mg - 2 (100) 2
Corporation limited Kenya THROZA 500mg - 1 (100) 1
Deva Holding Turkey Azitro 500mg 4 ((80) 1 (20) 5
EPHARM Ethiopia Ephazit 500mg - 1 (100) 1
Sandoz Romania Binozyt 500mg - 2 (100) 2
SHERYA LIFE Science India ZIT 500mg - 1 (100) 1
Umedica Laboratory India UZET 500mg - 1 (100) 1
ZIM Laboratory India Azito 500mg 1 (12.5) 7 (87.5) 8
Total 9 (23.7) 29 (76.3) 38
Ceftriaxone
Ashish life science India CEFTASH 1000mg 6 (100) - 6
Asralsteril Tech India ZEFONE100 1000mg 5 (100 - 5
BILIM pharmaceutical Turkey FORSEF 1000mg 2 (100) - 2
CSPC Zhougnuo Pharmaceutical China Ceftazone 1000mg 9 (100) - 9
Gulf pharmaceutical industry UAE Triaxon 1000mg 3 (100) - 3
Shandonglukang pharmaceutical China Ceftriaxone 1000mg 13 (100) - 13
Theon Pharmaceutical India THEOXONE 1000mg 2 (100) - 2
VHB MEDI Science limited India IVIXONE 1000mg 1 (100) - 1
Zhuhai Kinhoo pharmaceutical China Ceftriaxone 1000mg 1 (100) - 1
Total 42 (100) - 42

UAE: United Arab Emirates, UK: United Kingdom, APF: Addis pharmaceutical factory.

Factors that influence the potency of antibiotics

In the current study, among different factors assessed air condition of the pharmacy for amoxicillin (X2 = 4.27; p = 0.039), the source of all antibiotics (X2 = 5.41; p = 0.02), and the source of amoxicillin (X2 = 4.73; p = 0.03) were significantly associated with potency of antibiotics (Table 6).

Table 6. Factors that affect the potency of selected antibiotics collected from pharmacies found in Adama, Ethiopia (March 2018 to June 2018).

Variables Potency of antibiotics* X2 value p-value
Pass, n (%) Fail, n (%)
Type of pharmacy from where all antibiotics obtained Private 49 (48) 53 (52) 3.47 0.07
Government 14 (70) 6 (30)
Type of pharmacy from where amoxicillin was obtained Private 18 (52.9) 16 (47.1) 0.24 0.63
Government 5 (62.5) 3 (37.5)
Type of pharmacy from where ciprofloxacin was obtained Private 20 (58.8) 14 (41.2) 3.68 0.06
Government 8 (100) -
Type of pharmacy from where azithromycin was obtained Private 11 (32.4) 23 (67.6) 0.09 0.77
Government 1 (25) 3 (75)
Air condition of pharmacy for all antibiotics Ventilation 40 (55.6) 32 (44.4) 1.07 0.30
No ventilation 23 (46) 27 (54)
Air condition of pharmacy for amoxicillin Ventilation 17 (68) 8 (32) 4.27 0.039
No ventilation 6 (35.3) 11 (64.7)
Air condition of pharmacy for ciprofloxacin Ventilation 16 (64) 9 (36) 0.19 0.66
No ventilation 12 (70.6) 5 (29.4)
Air condition of pharmacy for azithromycin Ventilation 7 (31.8) 15 (68.2) 0.001 0.97
No ventilation 5 (31.3) 11 (68.7)
Shelf life for all antibiotics Long expired date 84 (55.3) 68 (44.7) 0.16 0.69
Near to expiry (<6mnth) 4 (33.3) 8 (66.7)
Shelf life for azithromycin Long Expiry date 9 (30) 21 (70) 0.160 0.69
Near to expiry date (<6mnth) 3 (37.5) 5 (62.5)
Source for all antibiotics Local 29 (53.7) 25 (46.3) 5.41 0.02
Foreign 76 69.1) 34 (30.9)
Source for amoxicillin Local 14 (45.2) 17 (54.8) 4.73 0.03
Foreign 9 (81.8) 2 (18.2)
Source for ciprofloxacin Local 11 (84.6) 2 (15.4) 2.97 0.85
Foreign 17 (58.6) 12 (41.4)
Source for azithromycin Local 4 (40) 6 (60) 1.67 0.51
Foreign 8 (28.6) 20 (71.4)
Awareness on unlicensed antibiotic distributer Yes 42 (53.2) 37 (46.8) 0.001 0.97
No 46 (54.1) 39 (45.9%)
Work experience < 10years 64 (52.9) 57 (47.1) 0.023 0.88
≥10 years 24(55.8) 19 (44.2%)

* Ceftriaxone was excluded from analysis because all of them (n = 42) were potent.

Discussion

Out of 164 antibiotics tested in this study, only 61% were found to be potent. The potency of antibiotics varies based on the countries of origin in which 53.7% and 54.6% of antibiotics from India and Ethiopia were potent respectively. Among the four categories of antibiotics tested, less than 50% of azithromycin were not potent with a mean inhibition zone diameter of 17.47±3.83 mm. The inhibition zone was unsatisfactory according to the standard inhibition zone set by the CLSI guideline (21–26 mm) [15]. The inhibition zone of azithromycin in this study was probably affected by the pH of the microbiological growth medium and its dissolubility in 95% ethanol alcohol diluents [16].

About 50% of amoxicillin and ciprofloxacin in the current study were not potent indicating some defect either in the antibiotics itself, storage, limitation of our laboratory methods, and antibiotics can be counterfeit or of substandard [17]. Similarly, bacteria isolated from the clinical specimen was reported to have reduced susceptibility to amoxicillin and ciprofloxacin [18,19]. Unlike this study, most of the amoxicillin tested in the Middle East was not counterfeit and contained the amount of ingredients claimed by the manufacturer [20,21].

This study revealed that the mean inhibition zone diameter of amoxicillin to be 14.2 ± 4 mm which is not in line with the finding reported from Ghana (16 ± 0.6mm) [22]. Moreover, most of the amoxicillin produced in Ethiopia (EPHARM) had a mean zone of inhibition of less than 12 mm which is below the standard set by the CLSI. The variation observed could be due to a difference in the manufacturer; most of the amoxicillin in this study was locally produced. The difference could also be attributed to the laboratory method used to determine the potency of antibiotics.

The mean inhibition zone of ciprofloxacin was 30.9 ± 4.2mm which is in the range set by CLSI. However, most of them were not potent. In this study, the mean inhibition zone of ceftriaxone was 32.7±1. According to CLSI inhibition zone range, all ceftriaxone antibiotics were potent. Several studies, which were conducted on different clinical isolates, indicated the effectiveness of ceftriaxone [18,19,23].

The potency of antibiotics can be affected by various factors. In the present study, the air condition of the pharmacy (X2 = 4.27; p = 0.039) and source of the antibiotics were significantly associated with the potency of antibiotics (X2 = 5.41; p = 0.02). According to this study, 52% of all antibiotics from private pharmacies were not potent. About 64% of amoxicillin stored in a pharmacy with no ventilator failed to pass the potency test indicating the importance of the ventilator in keeping the integrity of antibiotics stored in the pharmacy. Most of the antibiotics (46.3%) from the local source (Ethiopia) were not potent; specifically, 54.8% of amoxicillin from the local source was unable to pass the potency test (X2 = 4.73; p = 0.03). This could be due to problems that could arise during the production, shipment, and storage condition of antibiotics. Moreover, antibiotics could be of substandard or counterfeit which may contain active ingredients below the required level.

Limitation of the study

Only four antibiotics were tested, which might not be representative of other antibiotics. We faced a shortage of similar studies to compare the findings of this study.

Conclusions

About 60% of antibiotics tested in the current passed the potency test. The potency of antibiotics varies based on the source country where 53.7% and 54.6 of antibiotics from India and Ethiopia passed the potency test. Most of the azithromycin did not pass the potency test while all ceftriaxone passed the potency test. Among factors assessed, air condition of pharmacy, source of all antibiotics, and source of amoxicillin were significantly associated with potency of antibiotics. This study highlights the importance of further investigation to identify the magnitude of the problem and its causes at a large scale.

Supporting information

S1 File

(DOCX)

Acknowledgments

We would like to acknowledge the staff of the Oromia public health laboratory for facilitating laboratory work. We also acknowledge study participants for their willingness to participate in the study.

Abbreviations

CLSI

Clinical Laboratory Standard Institute

OPHL

Oromia Public Health Laboratory

ATCC

American type culture collection

SPSS

Statistical Package for Social Sciences

Data Availability

All data and materials are available with in the manuscript.

Funding Statement

The author(s) received no specific funding for this work.

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Decision Letter 0

Praveen Rishi

23 Apr 2021

PONE-D-21-05088

Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia

PLOS ONE

Dear Dr. Ali,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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We look forward to receiving your revised manuscript.

Kind regards,

Praveen Rishi, Ph.D., FAMI, FABMS

Academic Editor

PLOS ONE

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: No

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: I Don't Know

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: No

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: In this submitted manuscript   authors  claimed that about 40% of antibiotics tested in the present study were not potent and the potency of antibiotics varies based on the source of the country.  Authors also claimed that most of azithromycin were not potent while all ceftriaxone were potent.  Author (s) mentioned  that the physicochemical condition in the  pharmacy setup significantly associated with the potency of antibiotics.Manuscript is not technically sound due to poor presentation and   so it is very difficult  to understand what kind of message to give the author (s) in the present MS.   However, there are following  points that need to be addressed :1. What could be the scientific reason,  reduction in potency of antibiotic.?2. Does variation of API ( Source of API) in the antibiotics preparations responsible for antibiotic potency.3. Does the pharmacy set up awareness of this  type of loss in the potency of antibiotics?

Reviewer #2: Comments

This study about “Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia -” provides interesting data but has many shortcomings. These points should be addressed. My major comments are as follows.

1.The manuscript is not written so well and therefore, it is difficult to understand what authors want to say.

2.Language of the manuscript needs to be improved thoroughly. Some points, words or sentences have been highlighted in the manuscript and corrections should be made throughout the manuscript thoroughly.

3.On page number 13, E. coli must be italicized in table 3.

4. “To obtain 10 μg of amoxicillin disc, 500 mg of amoxicillin tablet was dissolved in 250 ml of phosphate buffer and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 5 μg of ciprofloxacin disc, 500mg of ciprofloxacin tablet was dissolved in 500ml of distilled water and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 30 μg of ceftriaxone, 1000mg of injectable ceftriaxone was dissolved in 166.7ml of distilled water and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 15 μg of azithromycin, 500mg of azithromycin the tablet was dissolved in a 166.7 ml of 95% ethanol with a broth media and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc.” Authors have used different volumes of different solvents and different amounts of antibiotics, justify.

5.“5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc”. What does “5 μm” mean? How authors confirmed/checked that 5 μm was impregnated on disc?

6.Present work describe the potency of antibiotics. In Table 4, what factors were considered to define/calculate potency of antibiotics on the basis of country?

7.Which factors define the pass and fail percentage of any antibiotic in Table 4 and 5?

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: NA

Reviewer #2: No

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PLoS One. 2021 Jul 1;16(7):e0253971. doi: 10.1371/journal.pone.0253971.r002

Author response to Decision Letter 0


3 May 2021

Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: No

Reviewer #2: Partly

________________________________________

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: I Don't Know

________________________________________

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

________________________________________

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: No

________________________________________

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: In this submitted manuscript authors claimed that about 40% of antibiotics tested in the present study were not potent and the potency of antibiotics varies based on the source of the country. Authors also claimed that most of azithromycin were not potent while all ceftriaxone were potent. Author (s) mentioned that the physicochemical condition in the pharmacy setup significantly associated with the potency of antibiotics. Manuscript is not technically sound due to poor presentation and so it is very difficult to understand what kind of message to give the author (s) in the present MS.

Response: Thank you for your valuable comments.

• In order to address the technical issue of the manuscript, we have included the following information in the method section: categories of antibiotics tested and their form (in the study design and population), Recommended storage condition of evaluated antibiotics, antibiotic disc preparation heading with detail description, antimicrobial susceptibility testing heading with detail description, pass criteria heading with detail description. We have also included details of what we did to maintain the quality of the data under Data quality control. All these are shown in the manuscript with track change.

However, there are following points that need to be addressed :1. What could be the scientific reason, reduction in potency of antibiotic.?2. Does variation of API ( Source of API) in the antibiotics preparations responsible for antibiotic potency.3. Does the pharmacy set up awareness of this type of loss in the potency of antibiotics?

Response:

• Yes, most of the antibiotics tested did not pass the potency test; several factors can be the reason for the failure. In addition to factors that are significantly associated with the potency of the antibiotics in the current study, other factors such as substandard, counterfeit, laboratory methods used can also affect the potency of antibiotics. There are also possibilities of illegal antibiotics in pharmacies. We have mentioned these reasons in the middle and as the end of the discussion section.

• The pharmacies are of about the ineffectiveness of antibiotics indirectly from customers (there is no improvement despite antibiotic intake). We have communicated the finding of this study to concerned bodies.

Reviewer #2: Comments

This study about “Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia -” provides interesting data but has many shortcomings. These points should be addressed. My major comments are as follows.

1. The manuscript is not written so well and therefore, it is difficult to understand what authors want to say.

Response: Thank you for your constructive comments.

• We agree with comment; we have revised the manuscript as shown in the track change.

2.Language of the manuscript needs to be improved thoroughly. Some points, words or sentences have been highlighted in the manuscript and corrections should be made throughout the manuscript

Response:

• We agree with comment; we have revised the languages as shown in the track change.

3.On page number 13, E. coli must be italicized in table 3.

Response: We italicized as suggested.

4. “To obtain 10 μg of amoxicillin disc, 500 mg of amoxicillin tablet was dissolved in 250 ml of phosphate buffer and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 5 μg of ciprofloxacin disc, 500mg of ciprofloxacin tablet was dissolved in 500ml of distilled water and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 30 μg of ceftriaxone, 1000mg of injectable ceftriaxone was dissolved in 166.7ml of distilled water and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc. To obtain 15 μg of azithromycin, 500mg of azithromycin the tablet was dissolved in a 166.7 ml of 95% ethanol with a broth media and 5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc.” Authors have used different volumes of different solvents and different amounts of antibiotics, justify.

Response: For preparation of antibiotics, we have followed CLSI guideline (CLSI guideline M_100S26, 2016, 26 ed, Table 6A, page 192). Preparation procedure is attached as supplement file.

5.“5 μm of dissolved stock antibiotic was impregnated on the 6 mm sized disc”. What does “5 μm” mean? How authors confirmed/checked that 5 μm was impregnated on disc?

Response: We agree with the comment and corrected as 5 μL.

6.Present work describe the potency of antibiotics. In Table 4, what factors were considered to define/calculate potency of antibiotics on the basis of country?

Response: We agree with the comment and included ‘pass’ and ‘fail’ criteria set by CLSI in the method section as shown in the track change.

7.Which factors define the pass and fail percentage of any antibiotic in Table 4 and 5?

Response: We agree with the comment and included ‘pass’ and ‘fail’ criteria set by CLSI in the method section.

Attachment

Submitted filename: Response to reviewers comments.docx

Decision Letter 1

Praveen Rishi

17 Jun 2021

Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia

PONE-D-21-05088R1

Dear Ali, 

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Praveen Rishi, Ph.D., FAMI, FABMS

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Partly

Reviewer #2: Partly

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: N/A

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Still the author must improve the language of the MS rigorously. Still it is very difficult to understand the MS due to poor presentation.

Reviewer #2: In line 147; “The uncertainty measurement for amoxicillin, ciprofloxacin, azithromycin, and ceftriaxone with a 95% CI were 17-19 mm, 31-32 mm, 21-24 mm, and 31-33 mm respectively.” What does “CI” refer to?

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Satish K Pandey

Reviewer #2: No

Acceptance letter

Praveen Rishi

21 Jun 2021

PONE-D-21-05088R1

Potency of commonly retailed antibiotics in pharmacies found in Adama, Oromia regional state, Ethiopia

Dear Dr. Ali:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Prof. Praveen Rishi

Academic Editor

PLOS ONE

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    Submitted filename: Response to reviewers comments.docx

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    All data and materials are available with in the manuscript.


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