Hospital-prepared low-dose atropine eye drops for myopia progression control using atropine sulfate injection diluted in normal saline and lubricants

Abstract

Background As commercial low-dose atropine eye-drops for myopia progression control are available in some countries, in-house preparation by diluting the 0.1% atropine eye-drop with sterile water or normal saline has been a common practice. Atropine injection is readily available and could be a more feasible alternative.

Objective To assess the properties of the in-house low-dose atropine eye-drops prepared by diluting the atropine injection in two solvents and tested in two temperature conditions.

Method The 0.01% atropine eye-drops (15ml) were prepared by diluting atropine sulfate injection with normal saline and lubricant eye-drops and stored at room temperature and in a refrigerator. All samples were daily dropped for 12 weeks to mimic real-life use, one of which was assessed every two weeks for the biological contamination and chemical properties. The active substance was compared with freshly prepared samples at the 12^th week.

Results The 0.01% atropine eye-drops contains no bacteria, fungi, or particulate matter. The levels of atropine sulfate on all samples were comparable to the freshly prepared samples at the 12^th week, regardless of the solvents used or storage conditions.

Conclusion The low-dose atropine eye-drops prepared from readily available atropine sulfate injection at healthcare facilities could be alternative to commercial products

Background

Myopia or short-sightedness is an ophthalmic condition that leads to blurred vision at distance, generally described by a refractive error of -0.5 diopter or less and a high myopia of -5.0 diopter or less [1]. The prevalence of myopia is increasing; as high as 50% of the world population would have some degree of myopia in 2050, of which about 5% will have high myopia which is associated with the risk of irreversible vision impairment and blindness due to pathological changes in the retina, choroid, and sclera [2].

Several behavioral modifications to delay the onset and retard of myopia progression, such as encouraging children to spend time outdoors, and limiting closed-vision activities have been recommended but might not be sufficient nor feasible [3]. Other interventions such as special spectacle or contact lens for myopia progression control also have limited practicality with questionable result in slowing progression of myopia [4].

As a non-selective muscarinic receptor antagonist, atropine has been used as a medical option for slowing myopia progression among children. Despite limited evidence on the exact mechanism of atropine in myopia control, the most plausible mechanism is that it acts directly or indirectly on the retina or scleral, inhibiting thinning or stretching of the scleral, and thereby eye growth. In 2012, Chia et al demonstrated that atropine 0.01% has comparable myopia control efficacy and minimal side effects compared with atropine at 0.1% and 0.5% [5]. Findings from the Atropine for the Treatment of Myopia studies (ATOM2), the 0.01% atropine eye drop could significantly slow the myopia progression by 50% with no clinically significant side effects [6]. The low-dose atropine was endorsed by the World Health Organization Western Pacific Region Meeting on Myopia [3].

Several commercial 0.01% atropine eye drops have been approved by the Food and Drug Administration for myopia progression control only in some countries. Hence, in-house preparation by diluting a commercial atropine sulfate eye-drop with sterile water [5–8] or balanced salt solution (normal saline) has been applied [9, 10]. A practical technique is drawing 0.1ml of 1% atropine sulfate eye-drop and injecting it into a 10ml bottle of either commercial artificial tear or balanced salt solution eye-drops. According to the package insert, the original 1% atropine sulfate eye-drop is anticipated to be stable for at least 36 months before opening and only 28 days after opening [9]. The shelf-life is expected to be shorter than one month after opening, which is not practical or economical for clinical practice as well as patient convenience and compliance in the long term.

Alternatively, we anticipated that the atropine sulfate injection commonly used for emergency treatment of bradycardia could also be used for the in-house preparation of the diluted atropine eye-drop for myopia progression control. Similar approach has been accomplished for antifungal (Voriconazole) [8] and immunosuppressive (Cyclosporine A and Tacrolimus) [7] sterile-water-based eye-drops. Atropine sulfate injection is readily available in any healthcare facility whereas the injection formulation usually contains no preservatives which are always of concern in the eye-drop formulation [10]. Moreover, the atropine sulfate injection could be measured and manipulated more easily than atropine sulfate eye-drop. Physical properties of the injection drug could be visually assessed before use whereas the opaque bottle of commercial eye-drop does not allow visual inspection.

As several solvent candidates such as sterile water, normal saline, and lubricant might affect the efficacy of the active substance, introduce some biological contamination, or change the chemical property of the final product, this study aims to investigate the physical, chemical, microbiological properties as well as the shelf-life of the 0.01% atropine eye-drop prepared by using the atropine sulfate injection diluted in two different solvents and tested in two temperature conditions.

Methods

The samples of low-dose atropine sulfate were prepared in normal saline solution (N) and lubricant eye-drops (L). The normal saline-based 0.01% atropine eye-drop was prepared by diluting 5 ml of atropine sulfate injection 0.6 mg/ml (GPO®, Lot J630218, Expiration June 2023) with 25 ml of 0.9% sodium chloride (GHP®, Lot 2010122, Expiration October 2022) to make a total volume of 30 ml then divided into two 15-ml bottles (Table 1). The lubricant-based 0.01% atropine eye-drop was prepared by diluting 2.5 ml of atropine sulfate injection 0.6 mg/ml (GPO®, Lot J630218, Expiration June 2023) with 12.5 ml of oxychloro complex (Purite®)-containing commercial lubricant eye drop (Cellufresh®, Lot T0780, Expiration August 2022) 12.5 ml to make a total volume of 15 ml. All these prepared samples were prepared in an isolator (ESCO®, Model LAC-6A1) at room temperature (15–25^◦C) and 40–65% humidity. Then they were allocated at 15 ml into PET bottles sterilized by an ethylene-oxide gas method except samples diluted with Cellufresh® which were prepared bottle by bottle. All the above samples were prepared for 24 bottles of each diluent.

The samples were kept in two storage conditions: room temperature (R) and refrigerator (F) (Sanyo®, Model MPR-720), therefore, four groups underwent the study (NR, NF, LR, LF) (Table 1). All samples were daily dropped for six months to mimic real-life use. The samples underwent biological contamination assessment methods that complied with Chap. 71 of the United States Pharmacopeia (42nd edition). Every 14 days, each scheduled sample of each group was collected 10 mL and was sent to the laboratory department, Bumrungrad International Hospital until six months (Table 2). At the 12th week, all samples were sent to perform an assay test at CET-Scientific Services Pte. Ltd., Singapore using liquid chromatography with UV 225 nm detector, 4.6 mm x 15 cm; 5-µm packing L10 column at 40ºC, flow rate 1.2 ml/min, injection volume 20 µl with running time not less than 3 times the retention time of atropine.

Results

The culture of Aerobic bacteria (Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa), anaerobic bacteria (Clostridium sporogenes), and fungi (Candida albicans, Aspergillus brasiliensis, Aspergillus Niger) had no growth. There was no particulate matter found in all samples and no change in color of all samples. All samples at the 12th week, regardless of the solvents used or storage conditions had comparable levels of the atropine sulfate to the freshly prepared samples (Table 2).

Discussion

Atropine sulfate of the prepared products remained at a similar quantity to the freshly prepared, regardless of the solvents used and the storage condition after three months. No biological contamination or particulate matter was detected. The findings suggested no significant effect of both solvents or storage conditions on remaining amounts of active substance in samples including the effect on physical properties of samples.

Our experiment concurs with previous studies on in-house antifungal [8] and immunosuppressive [7] eye-drop preparations. We also demonstrate similar efficacy of atropine sulfate in various solvents. Sterile water has been a common solvent used in many ophthalmic drug preparations [5–8] whereas normal saline is increasingly been used [9, 10]. In 2019, Saito et al demonstrated the physical, chemical, and microbiological stability of the in-house prepared atropine sulfate eye-drops by diluting the 1% atropine sulfate (10 mg/ml) eye-drop with normal saline to have 0.01, 0.1, 0.25, and 0.5% atropine sulfate for as long as 6 months [9].

Our study is the first to comparatively assess the properties of in-house atropine sulfate eye-drops preparation in two different solvents: normal saline and lubricant. The finding is useful supporting evidence for generalizability as the normal saline injection is more commonly available than the sterile water injection and that atropine sulfate injection is easily measured and manipulated as well as readily available in any healthcare facility. The type of solvents seems to have no effects so the clinician could choose the most appropriate solvent for each patient. In some patients who also need lubricating effect, a commercial lubricant eye-drop could be used as a solvent with comparable results.

The in-house preparation of the 0.01% atropine eye-drop would have been assumed to be stable for only 28 days after opening as described in the package insert should the commercial 1% atropine eye-drop be used. The atropine sulfate injection used in our study is proved to be beneficial for practical use as the prepared product could be refilled every three months which is more convenient and economical for the patient than the monthly refill.

Several limitations of our study should be noted. First, although our study suggested that the shelf life of the product could last for three months after opening in the simulated conditions, this range might be shortened by possible contamination in the real-life use especially in a poor hygiene place. Second, some chemical properties such as pH and osmolarity were not formally assessed because of the limited funding. Atropine sulfate could be degraded and make the product more acidic and unstable; however, findings from a recent study suggested that the pH of the prepared product could be stable for almost 6 months [10].

Conclusion

The low-dose atropine eye-drops prepared from readily available atropine sulfate injection at healthcare facilities could be alternative to commercial products.

Declarations

The authors declare that they have no conflicts of interest.

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