📷 By Jayo Santiago/ Flickr

PhLE Review Day 1 💊👨‍💻👨‍🔬📚

house, online, self review

27 May 2024

I set a schedule for us trio to have a preparation for the board exam 3 years after. It is better to be prepared ahead of time, so that it will be easy for us to study in review centers or institutes. 👨‍💻📚 MONDAY: Pharmaceutical Calculations and Inorganic Chemistry

Middle Term Diaries 1/n 💊🏫

house at midnight

02 July 2024

After finishing the laboratory reports that I assigned to myself, I reviewed for my midterm exam in Medicinal Organic Chemistry even though I felt lazy to review.

Laboratoire 7/n 🥼

Laboratory

11 November 2023

An experiment on Test on Lipids, a challenge in my part because I have to recall some laboratory techniques in which I forgot for the past 4 years. Thankfully, my ading assisted in on how to use some of the apparatus because it's been 4 years since the last time I performed techniques in the laboratory. 👨‍🔬🥽🥼🧪

📸 Debbie

BOTICA DIARIES (Epilogue) 💊

Rosales, Pangasinan

throughout my 1 year and 2 months career (2022-2023)

Today, 2024-07-07, I was organizing the package inserts of the medicines that I got from its respective boxes when I was working at the pharmacy. Having these kinds of documents were an advantage to me because I am kind of reviewing also the brand names of different drugs and their corresponding indications. I never regret getting these, it will help me in reviewing for my licensure examination.

Salt formation: an effective means to improve the physical and chemical properties of drug molecules and enhance the druggability of drugs

In drug development, drug forming research, including pharmacodynamics, pharmacokinetics, and early safety evaluation of drugs, is required to determine whether the active compound has the potential to be developed into a pill. The drug-forming properties of drugs are also an essential part of the drug-forming evaluation, and salt formation is one of the effective means to improve the physicochemical properties of drug molecules and enhance drug-forming properties.

Many drugs are salts of organic acids or bases. The salt formation can make some oily organic acids or organic bases solid, which is conducive to preparing concrete dosage forms. Moreover, the salt formation of drugs increases the water solubility, which is conducive to preparing some aqueous dosage forms, such as water injection and oral liquid. The salt formation process is often a purification process, which removes the impurities mixed in the drug that cannot become salt, etc. So what are the benefits of salt formation in drug development studies?

1,Salt formation of drugs can change the solubility of drugs and improve drug-forming properties

The solubility of drugs affects their pharmacokinetic properties, chemical stability, and the choice of dosage form, which is an essential element in evaluating drug-forming properties. A salt formation can change the solubility of drugs and improve the water solubility of drugs through salt formation, which is the primary method to develop intravenous injections of drugs, such as the poor water solubility of diuretic etanercept, which is mainly available in tablet form.

Still, its sodium salt has better water solubility and can be used to prepare intravenous injections. The free base of the antipsychotic haloperidol is also marketed mainly as a tablet due to its low solubility. At the same time, its lactate can be used to prepare injectable solutions with improved solubility.

Sometimes it is necessary to prepare extended-release dosage forms by reducing the solubility of the drug. In this case, it is required to form a salt of the drug with an acid or base of higher relative molecular mass and hydrophobicity. For example, the commercially available dosage forms of antidepressant trazodone hydrochloride are tablets, oral solutions, etc. The study of trazodone in salt found that its p-toluenesulfonate and dihydroxynaphthalate are much less soluble in water than sulfate, and hydrochloride p-toluenesulfonate is more suitable for the preparation of slow-release oral formulation.

2,Salt formation can improve drug stability

Formulation evaluation also needs to rely more on data generated from pre-prescription research work, such as extreme pH, high temperature, freeze-thaw, light, forced oxidation, and other forced degradation experiments to understand the stability of drugs. Medicilon offers a full suite of chemical drug development services integrated from start to finish. We provide a one-stop service through pre-prescription studies, drug analysis, drug stability studies, formulation development, and complete CMC services.

The stability of the drug is directly related to its dosage form and the selection of production and packaging conditions, and it even affects the effect of the final preparation. Some researchers chose the insoluble phenazopyridine (PAP) as a model drug and improved the solubility and stability of phenazopyridine through drug co-crystals and salts.

The marketed product of phenazopyridine is phenazopyridine hydrochloride. Still, the peak plasma concentration in rats is only 10-20 ng after 200 mg dose administration, and it is for these reasons that the clinical application of PAP is limited. Therefore, the investigators prepared one eutectic formed by phenazopyridine with phthalimide (1) and two salts with 4-hydroxyphenyl acetic acid (2) and saccharin (3) by solution method and spiked grinding method, respectively, and their structures obtained by X-ray single crystal diffraction showed the presence of hydrogen bonding between phenazopyridine and all three eutectic ligands, collectively called hydrogen bonding complexes [1].

X-ray powder diffraction, DSC, and IR characterized it. The powder solubility of the three hydrogen-bonded complexes was measured, and the hygroscopicity of the solid powders was examined at 85% and 98% relative humidity for 1, 3, 5, 7, 10, 14, 21, and 28 days. The experimental results showed that the melting points of the three hydrogen-bonded complexes were all between phenazopyridine and eutectic ligands; the powder solubility of 1-3 was 10, 7.5, and 2 times that of PAP, respectively; the hygroscopicity was much lower than that of PAP and its hydrochloride under the conditions of 85% and 98% relative humidity. According to the above results, it is clear that 1-3 has a good prospect for improving the bioavailability and stability of phenazopyridine.

3,Salt formation can change drug compliance

Drug formulation should be safe, effective, stable, and easy for patients to accept, i.e., good compliance. An essential indicator of compliance with oral formulations is the acceptability of taste, which is particularly important when the drug is administered in liquid, chewable, or effervescent dosage forms. For example, the prerequisite for oral drugs to produce a taste response must first be dissolved in the mouth or taken in solution. Therefore, one of the ways to reduce the bitterness of orally administered drugs is to make them into poorly soluble salts and to make their saturated concentration below the threshold for producing taste sensation.

4,Into salt, can extend the patent protection of the drug or circumvent its patent protection

In the R&D process of new drugs, once an active compound is discovered, it is generally applied for a patent on its chemical structure to ensure the novelty of the patent. After the drug is marketed, the developer will further develop its derivatives, such as making salts or changing the crystal form and dosage form, and file subsequent patent applications to obtain the longest possible patent protection period. Nowadays, most new drugs marketed internationally use this type of patent protection.

In addition, drug salting can reduce adverse effects. In developing salt-forming drugs, the key is to select the acid or base with which the drug is salted. The selection of the acid or base should consider its pKa value and safety, as well as the route of administration and dosage form after salting. In conclusion, drug-forming studies and drug-forming evaluations can be conducted to determine the drug-forming properties of drugs better and improve the efficiency of new drug development.

[1] Improvement of solubility and stability of phenazopyridine by drug eutectic and salt [J]

Random thoughts 1/n 💭

Tomorrow is my asynchronous class in Medicinal Organic Chemistry, I'm going to finish the remaining activities there and at the same time my assignment in Pharmacy Informatics to be submitted at noon. However, I'm craving coffee again after drinking it a few moments ago which makes me want to go to cafe tomorrow, but I don't have money to buy coffee XD. I'll make sure to finish the other tasks to eliminate workload.

2024.18.6

The last two days were not what I wanted. I suffered from terrible pain in my teeth. I did not go to the doctor at first, but after that I could not bear it, and when I went, it turned out that I had a tooth infection. He gave me medication, but I am still in pain, and I have exams on Monday coming up. I feel that small things have accumulated and spoiled my entire mood. Anyway, I will try to study today

So :

1. lecture four

2. lecture five

From pharmaceutical principles

BOTICA Diaries 6/n 💊

Rosales, Pangasinan

31 August 2022

7, 9 September 2022

The time I settled for a very long time in Rosales as pharmacy assistant. I started created bunch of memories there as I go back after 2 weeks of being assigned in one of our branches in Bayambang. I experienced night walks with my workmates to buy foods while raining, went to the municipal hall for a tour, ate dinner with them upstairs, and played hide and seek in the public market at night.

Just finished a hellish week in my life studying for 2 quizzes and 1 exam. I think that one of the worst feelings in the world is studying until you drop, then finding out you got points off on a quiz because of a silly mistake.

Point is: I need to sleep more 😭