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A Textbook of Clinical Pharmacology and Therapeutics

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● Introduction: ocular anatomy, physiology <strong>and</strong><br />

biochemistry 423<br />

● General pharmacokinetics <strong>of</strong> intra-ocular drug<br />

administration 423<br />

● Drugs used to dilate the pupil 423<br />

● Drugs used to constrict the pupil <strong>and</strong> to<br />

treat glaucoma 425<br />

INTRODUCTION: OCULAR ANATOMY,<br />

PHYSIOLOGY AND BIOCHEMISTRY<br />

CHAPTER 52<br />

DRUGS AND THE EYE<br />

The eye is protected by a series <strong>of</strong> barriers, namely the<br />

blood–retinal, blood–aqueous <strong>and</strong> blood–vitreous barriers, <strong>and</strong><br />

so represents both an opportunity for localized drug administration<br />

<strong>and</strong> also a challenge to drug delivery. See Figure 52.1 for<br />

a cross-sectional view <strong>of</strong> the anatomy <strong>of</strong> the eye.<br />

The structures <strong>of</strong> the eye itself are divided into the anterior <strong>and</strong><br />

posterior segments. The anterior segment includes the cornea,<br />

limbus, anterior <strong>and</strong> posterior chambers, trabecular meshwork,<br />

Schlemm’s canal, the iris, lens <strong>and</strong> the ciliary body. The posterior<br />

segment consists <strong>of</strong> the sclera, choroid, retina, vitreous <strong>and</strong> optic<br />

nerve. The anterior surface <strong>of</strong> the eye is covered by the conjunctiva.<br />

The ocular secretory system is composed <strong>of</strong> the main lacrimal<br />

gl<strong>and</strong> located in the upper outer orbit, <strong>and</strong> accessory gl<strong>and</strong>s<br />

located in the conjunctiva. The lacrimal gl<strong>and</strong> has both sympathetic<br />

<strong>and</strong> parasympathetic innervation. Parasympathetic innervation<br />

is relevant in that many drugs with anticholinergic side<br />

effects cause the symptom <strong>of</strong> dry eyes (see Table 52.1). Tear<br />

drainage starts through small puncta located in the medial aspects<br />

<strong>of</strong> the eyelids. Blinking causes tears to enter the puncta <strong>and</strong> drain<br />

through the canaliculi, lacrimal sac <strong>and</strong> nasolacrimal duct into the<br />

nose. The nose is lined with highly vascular epithelium which permits<br />

direct access <strong>of</strong> absorbed drugs to the systemic circulation.<br />

Consequently, even though the dose administered as eye drops is<br />

much smaller than the usual dose <strong>of</strong> the same drug (e.g. timolol)<br />

administered by mouth, the lack <strong>of</strong> first-pass metabolism may<br />

nonetheless lead to unwanted systemic effects.<br />

THE IRIS AND CILIARY BODY<br />

In the iris, dilator smooth muscle is orientated radially <strong>and</strong> innervated<br />

by the sympathetic system, which produces dilatation<br />

● Drugs used to treat eye infections 427<br />

● Drugs used to treat inflammatory disorders in<br />

the eye 427<br />

● Drugs for age-related macular degeneration 428<br />

● Local anaesthetics <strong>and</strong> the eye 428<br />

● Adverse effects on the eye <strong>of</strong> systemic drug therapy 428<br />

● Contact lens wearers 429<br />

(mydriasis). At the pupillary margin, the sphincter smooth<br />

muscle is organized in a circular orientation with parasympathetic<br />

innervation which, when stimulated, leads to pupillary<br />

constriction (miosis) (see Table 52.1 for a summary <strong>of</strong> the autonomic<br />

pharmacology <strong>of</strong> the eye).<br />

The ciliary body serves two specialized functions, namely<br />

secretion <strong>of</strong> the aqueous humour <strong>and</strong> accommodation.<br />

Parasympathetic stimulation contracts the ciliary muscle <strong>and</strong><br />

allows the lens to become more convex, focusing on near objects.<br />

Contraction <strong>of</strong> this muscle also widens the spaces in the trabecular<br />

meshwork <strong>and</strong> this also explains, in part, the effect <strong>of</strong><br />

parasympathomimetics in lowering intra-ocular pressure.<br />

GENERAL PHARMACOKINETICS OF<br />

INTRA-OCULAR DRUG ADMINISTRATION<br />

The bioavailability <strong>of</strong> intra-ocularly administered drugs<br />

depends on pH <strong>and</strong> other pharmaceutical properties <strong>of</strong> the<br />

vehicle. Most ophthalmic drugs in general use are delivered as<br />

drops, usually in aqueous solution. Formulations which prolong<br />

the time for which a drug remains in contact with the eye surface<br />

include gels, ointments, solid inserts, s<strong>of</strong>t contact lenses <strong>and</strong> collagen<br />

shields. Drug penetration into the eye itself is approximately<br />

linearly related to the concentration <strong>of</strong> drug applied.<br />

Nasolachrymal drainage plays a key role in the systemic<br />

absorption <strong>of</strong> drugs administered to the eye, <strong>and</strong> drugs<br />

absorbed via this route circumvent hepatic first-pass metabolism.<br />

Thus ocular drugs such as β-adrenergic antagonists can<br />

cause wheezing in asthmatic patients. Figure 52.2 shows<br />

potential pathways for drug absorption in the eye.<br />

DRUGS USED TO DILATE THE PUPIL<br />

Mydriasis (pupillary dilatation) is <strong>of</strong>ten required for detailed<br />

examination <strong>of</strong> the retina. Two major groups <strong>of</strong> drugs are used

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