Physical Pharmacy and Jurisprudence & Ethics High-Yield Review

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Description and Tags

Vocabulary practice flashcards covering essential physical pharmacy concepts and Philippine jurisprudence and ethics regulations for pharmacy board examinations.

56 Terms

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Physical Pharmacy

The branch of pharmaceutical science that applies physical and chemical principles to study the physicochemical properties of substances used in pharmaceutical formulation.

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Keesom Forces

Intermolecular van der Waals forces caused by permanent dipole–dipole interactions (orientation effect).

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Debye Forces

Intermolecular van der Waals forces produced when a permanent dipole induces a dipole in an adjacent molecule (induction effect).

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London Forces

Intermolecular van der Waals forces arising from temporary induced dipole–induced dipole interactions (dispersion effect), essential for nonpolar interactions and liquefaction of gases.

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Additive Property

A physical property that depends on the total combined contribution of all atoms within a molecule (e.g., molecular weight, mass).

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Constitutive Property

A physical property that depends on the specific structural arrangement and bonding of atoms in a molecule (e.g., refractive index, optical rotation).

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Colligative Property

A property of a solution that depends strictly on the total number of dissolved solute particles rather than their chemical identity (e.g., vapor-pressure lowering, freezing-point depression).

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Intensive Property

A physical property that remains independent of the total quantity of matter present (e.g., temperature, pressure, density, viscosity, surface tension, specific gravity).

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Extensive Property

A physical property that varies directly with the amount or size of the system (e.g., mass, length, volume).

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Triple Point

The specific state of temperature and pressure at which the solid, liquid, and gaseous phases of a substance coexist simultaneously in equilibrium.

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Critical Point

The point on a phase diagram at which the boundary between liquid and gas ceases to exist and the two phases become indistinguishable.

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Gibbs Phase Rule

The phase equilibrium relationship expressed as F=C−P+2F = C - P + 2 for a one-component system, where FF is degrees of freedom, CC is number of components, and PP is number of phases.

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Smectic Liquid Crystals

A mesophase state characterized by elongated molecules aligned in definite parallel layers with soap-like flow properties.

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Polymorphism

The ability of a chemical substance to crystallize into more than one distinct crystalline form with differing physical properties such as solubility and melting point.

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Enantiotropic Polymorphs

Polymorphic forms of a substance that can reversibly transform into one another at a specific transition temperature.

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Monotropic Polymorphs

Polymorphic forms where the phase transition between forms is strictly unidirectional and irreversible, proceeding from a metastable form to the stable form.

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Theobroma Oil Polymorphs

Four crystal modifications of cocoa butter: gamma (18∘C18^\circ\text{C}, least stable), alpha (22∘C22^\circ\text{C}), beta-prime (28∘C28^\circ\text{C}), and beta (34.5∘C34.5^\circ\text{C}, most stable).

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Henry's Law

A gas law stating that at constant temperature, the mass of gas dissolved in a given volume of liquid is directly proportional to the partial pressure of that gas (C=kPC = kP).

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Graham's Law

A law establishing that the rate of diffusion or effusion of a gas is inversely proportional to the square root of its molecular weight: Rate1Rate2=MW2MW1\frac{\text{Rate}_1}{\text{Rate}_2} = \sqrt{\frac{\text{MW}_2}{\text{MW}_1}}.

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Micromeritics

The science and technology of small particles, covering both fundamental properties (size, shape, true volume) and derived properties (bulk density, porosity).

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Feret's Diameter

An optical microscopy particle measurement defined as the distance between two parallel tangents along opposite sides of the particle.

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Martin's Diameter

An optical microscopy dimension determined as the length of a line that divides the projected area of a particle into two equal halves.

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Angle of Repose

A parameter for evaluating powder flowability calculated using tan⁡(θ)=hr\tan(\theta) = \frac{h}{r}, where smaller angles denote better flow and steeper angles indicate poor flow.

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Carr's Index (CI)

A compressibility percentage derived as CI=[ρtapped−ρbulkρtapped]×100\text{CI} = \left[\frac{\rho_\text{tapped} - \rho_\text{bulk}}{\rho_\text{tapped}}\right] \times 100, where lower values represent superior flowability.

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Hausner Ratio (HR)

A flow predictor calculated as HR=ρtappedρbulk\text{HR} = \frac{\rho_\text{tapped}}{\rho_\text{bulk}}, where values closer to 1.001.00 to 1.111.11 indicate excellent powder flow.

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Zeta Potential

The electrokinetic potential existing at the slipping plane of a charged colloidal particle; lower magnitudes diminish repulsion and favor flocculation.

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Peptization

The process of redispersing or converting a coagulated precipitate back into a stable colloidal dispersion.

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Caking

A suspension instability characterized by the formation of a dense, highly compact sediment that resists redispersion upon shaking.

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Coalescence (Cracking)

An irreversible emulsion failure where dispersed droplets fuse together into larger globules, resulting in complete phase separation.

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Syneresis

The spontaneous contraction of a gel structure resulting in the outward expulsion of liquid from the gel network.

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Sodium Chloride Equivalent (E-value)

The weight of sodium chloride in grams that produces an equivalent osmotic effect to 1 g1\,\text{g} of a specific drug substance.

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White–Vincent Method

A Class II tonicity adjustment method that calculates the volume of water needed to yield an isotonic solution (V=[weight×E]×111.1V = [\text{weight} \times E] \times 111.1) before diluting with an isotonic vehicle.

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Buffer Capacity (β\beta)

A quantitative measure of buffer resistance to pH change, calculated as the ratio of strong acid or base equivalents added per liter to the resulting change in pH.

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Shelf-Life (t90t_{90})

The duration of storage required for the concentration of an active drug ingredient to decline to 90%90\% of its original label potency (10%10\% degraded).

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Thixotropy

A time-dependent reversible non-Newtonian flow behavior where viscosity decreases under continuous shear stress and gradually recovers when the stress is removed.

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Rheopexy

A time-dependent non-Newtonian rheological property where viscosity increases over time under continuous applied shear stress.

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Autonomy

A universal bioethical principle obligating practitioners to respect a patient's self-determination, informed consent, and voluntary choices without coercion.

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Veracity

The bioethical principle of honesty and full disclosure of relevant medical and medication information to patients and colleagues.

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Beneficence

The bioethical duty to act affirmatively for the benefit, health, and welfare of the patient.

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Nonmaleficence

The core bioethical mandate to 'do no harm' and proactively prevent foreseeable medication errors or treatment-related injuries.

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Role Fidelity

The bioethical commitment to practice within defined professional standards, competencies, ethical responsibilities, and statutory boundaries.

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Republic Act No. 5921

The historical Pharmacy Law governing pharmaceutical education, licensing, the Board of Pharmacy, and the professional regulation of pharmacy practice in the Philippines.

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Republic Act No. 6675

The Generics Act of 1988, mandating the use of generic terminology across prescribing, dispensing, manufacturing, advertising, and distribution of medicines.

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Republic Act No. 8203

The Special Law on Counterfeit Drugs, prohibiting and penalizing the manufacture, distribution, dispensing, and trafficking of counterfeit medications.

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Republic Act No. 9165

The Comprehensive Dangerous Drugs Act of 2002, repealing RA 6425 and governing dangerous drug control, licensing, enforcement, the DDB, and the PDEA.

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Republic Act No. 9711

The Food and Drug Administration (FDA) Act of 2009, which modernized and strengthened the former BFAD and officially renamed it the Food and Drug Administration.

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Republic Act No. 7581

The Price Act, which provides consumer protection against arbitrary price hikes and outlaws illegal price manipulation schemes such as hoarding, profiteering, and cartels.

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Erroneous Prescription

A prescription containing generic naming where the format violates rules (e.g., brand name precedes generic, generic is enclosed in parentheses, or brand name is not in parentheses); must be retained and reported.

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Violative Prescription

A prescription where the generic name is missing, illegible while the brand name is visible, or where 'no substitution' instructions prevent generic dispensing; must not be filled as written.

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Impossible Prescription

A prescription where only an illegible generic is written, generic and brand names do not correspond, both are illegible, or the drug is not FDA-registered; must not be dispensed.

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Philippine Drug Enforcement Agency (PDEA)

The primary operational and implementing arm responsible for enforcing the regulatory and penal provisions of RA 9165 regarding dangerous drugs.

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S2 License

A specialized permit issued by PDEA that authorizes registered physicians, dentists, or veterinarians to prescribe dangerous drug preparations.

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Dangerous Drug Prescription Retention

The legal requirement under RA 9165 modules directing community and institutional pharmacists to preserve original dangerous drug prescriptions on file for five years.

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Hoarding

The illegal practice penalized under RA 7581 involving the undue accumulation or intentional withholding of basic necessities or prime commodities from regular trade channels.

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Profiteering

An unlawful trade practice under RA 7581 defined as the sale or offering for sale of any basic necessity or prime commodity at an excessively high price.

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Cartel

Any unlawful combination, agreement, or conspiracy among competitors, producers, or sellers organized to manipulate, control, or artificially inflate prices.