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1
Buffered and Isotonic Solutions
2
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
3
Introduction
Buffered Solutions ?
4
Buffered Solutions
0.1N HCl 1ml
pH4.7
H2O NaCl HAc,NaAc
pH7 pH7
3 3 4.58buffer action
5
Buffered Solutions
HA + OH- A- + H2O
A- + H3O+ HA + OH-
• Combination of a weak acid and its conjugate base
• Combination of a weak base and its conjugate acid
6
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
7
The Buffer Equation • A Weak Acid and Its Salt
H3O+ + Ac-HAc + H2O
-log[H3O+]= - logKa - log[acid] + log[salt]
salt
acid Ka =
[H3O+][Ac-]
[HAc]
K1[HAc][H2O] = K2[H3O+][Ac-]
8
The Buffer Equation
• A Weak Acid and Its Salt
pH= pKa+log [salt] [acid]
Buffer equation orHenderson-Hasselbalch equation
Dissociation exponent
9
Common ion effect
H3O+ + Ac-HAc + H2O
* when Sod. acetate is added to acetic acid…
is momentarily disturbed since the acetate ion supplied by the salt increases the [Ac-]
Ka =[H3O+][Ac-]
[HAc]
The ionization of HAc is repressed upon the addition of the common ion [Ac-]
10
The Buffer Equation • A Weak Base and Its Salt
Kb =[OH-][BH+]
[B]
OH- + BH+B + H2O
salt
base
11
The Buffer Equation
• A weak base and its salt
[H3O+] • [OH-] = Kw
[OH-] = Kb [base][salt]
-log[H3O+]= - logKw – log1/Kb - log[salt]/[base]
12
The Buffer Equation
• A Weak Acid and Its Salt
pH= pKw- pKb + log [base] [salt]
* Buffers are not ordinarily prepared from weak bases because of the volatility & instability of the bases and because of the dependence of their pH on pKw, which is often affected by temp. changes.
13
Activity coefficients
H3O+ + Ac-HAc + H2O
aH3O+ •aAc-
aHAc
Ka =[H3O+][Ac-]
[HAc] =
(γH3O+•cH3O+)•(γAc-• CAc-)
(γHAc•CHAc)=
Molar conc.
Activity coeffi-cients
Conc. activ-ity
activity
14
Activity coefficients
aAc-
aHAc
- log[aH3O+] = - log Ka + log
* activity coefficient of the undissociated acid γHAc is essentially 1 and may be dropped.
[salt][acid]
pH = pKa + log + log γAc-
15
pH 에 영향 주는 인자
1. Altering the ionic strength
① Addition of neutral salts
② Dilution (alter activity coefficients)
The pH of the most basic buffer was found to change more markedly with temp. than that of acid buffers, owing to Kw.
2. Temperature
16
pH indicator
• Acid indicator 의 경우
HIn + H2O H3O+ + In-
Alkaline colorAcid color
KIn = [H3O+ ][ In-]
[HIn]
base
acid
17
PH indicator
• pH = pKIn + log [base][acid]
1/10~10/1
pH =pKIn + 1
base acid10/1 1/10
* From experience, one cannot discern a change from the acid color to the salt color the ratio of [base] to [acid] is about 1 to 10
* The effective range of the indicator is…
18
pH indicator
• Characteristics of colorimetric method
① less accurate
② less convenient but less expensive than elec-trometric method
③ difficult to apply for the unbuffered pharma-ceutical preparation (change the pH -indicator itself is acids or base)
④ error may be introduced by the presence of salts & proteins
19
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
20
Buffer capacity
β= B pH
ΔB : small increment in gram equivalents/Liter of strong(or acid) added to the buffer
soln. to produce a pH change of ΔpH
buffer capacity= buffer efficiency
= buffer index= buffer value
• …the magnitude of the resistance of a buffer to pH changes
21
Buffer capacity ( 근사식 이용 )HAc
(0.1- 0.01)
NaAC(0.1+ 0.01)0.01
+ NaOH + H2O
pH=pKa + log [salt] + [base][acid] - [base]
= 4.85
pH=pKa + log[salt][acid] = 4.76
=0.01
0.09= 0.11=
pH β
B
• Before the addition of NaOH
• After the addition of NaOH
22
• A more exact equation for buffer capacity (1914, 1922)
Buffer capacity
β ---- at any [H3O+].
Ka • [H3O+]β = 2.3 • C •
(Ka + [H3O+])2
c : total buffer conc.(sum of the molar conc. of
the acid & the salt)
23
• βmax occurs where pH = pKa ([H3O+] = Ka)
Maximum Buffer capacity
( pH = pKa )
βmax = 0.576 • C
42.303
• C[H3O+]2
βmax = 2.303 • C • (2 [H3O+])2
=
24
Characteristics of Buffer Ca-pacity
• …is not a fixed value, but rather depend on the amount of base added
• …depends on the value of the ratio [salt]/[acid] and magnitude of the individual concentrations of the buffer components
• The greatest capacity(βmax) occurs where [salt]/[acid] = 1 and pH = pKa
• Because of interionic effects, buffer capacities do not in general exceed a value of 0.2
25
• Total buffer capacity of a universal buffer (combination of several buffers)
Universal Buffer
26
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
27
In Vivo biologic buffer systems
• Blood
① Primary buffers : Plasma ;
NaHCO3-- H2CO3, NaHPO4--NaH2PO4, protein
② Secondary buffers : Erythrocytes ;
hemoglobin-oxyhemoglobin, K2Hpo4--KH2PO4
• Lacriminal fluid
- pH: 7.4 (range 7 – 8 or slightly higher)
• Urine
- pH: 6.0 (range 4.5 – 7.8)
- below normal…hydrogen ions are excreted by the kidney.
- above pH 7.4…hydrogen ions are retained by action of the kid-ney.
28
Pharmaceutical buffers
• ophthalmic soln.
• colormetric determination of pH
• research studies in which pH must be held constant
29
Pharmaceutical buffers
• Clark-Lubs mixtures and pH
(a) HCl & KCl, pH 1.2 - 2.2
(b) HCl & potassium biphthalate, pH 2.2 - 4.0
(C) NaOH & potassium biphthalate, pH 4.2 - 5.8
(d) NaOH & KH2PO4 , pH 5.8 - 8.0
(e) H3BO3, NaOH & KCl, pH 8.0 - 10.0
30
Preparation of pharmaceutical buffer so-lutions
• Steps for development of a new buffer
① Select a weak acid having a pKa approximately equal to the pH at which the buffer is to be used.
② Calculate the ratio of salt & weak acid required to ob-tain the desired pH.
③ Consider the individual conc. Of the buffer salt & acid needed to obtain a suitable buffer capacity
* Individual conc. : 0.05 ~ 0.5M * buffer capacity : 0.01 ~ 0.1
31
Preparation of pharmaceutical buffer so-lutions
• Steps for development of a new buffer
④ Availability of chemicals, sterility of the final soln, stabil-ity of the drug & buffer, cost of materials, freedom from toxicity
ex) borate buffer – toxic effect – not be used for oral or parenteral products.
⑤ Determine the pH and buffer capacity using a reliable pH meter
32
Buffer in pharmaceutical and biologic sys-tems
• Influence of buffer capacity and pH on tissue ir-ritation
* Tissue irritation will be minimal when…
(a)Buffer solution – β , Volume (b) Physiologic fluid - β , Volume
33
Buffer in pharmaceutical and biologic sys-tems
• Stability vs. optium therapeutic response
* Undissociated form of a weakly acidic or basic drug has a higher therapeutic activity than the dissociated salt form.
* Molecular form is lipid soluble & can penetrate body membranes readily, where the ionic form, not being lipid soluble, can penetrate membranes only with greater dif-ficulty.
34
Buffer in pharmaceutical and biologic sys-tems• pH and solubility
* Influence of buffering on the solubility of base
- At a low pH : base is in the ionic form & usually very sol-uble in aqueous media
- As the pH is raised : more undissociated base is formed when the amount of base exceeds the limited water solubil-ity of this form, free base precipitates from soln.
Base soln. should be buffered at a sufficiently low pH for stabilization against precipitation.
35
(Example)
GOAL: Compute the mole percent of free base present on 25 and at a ℃
pH of 7.4. The pKb of pilocarpine is 7.15 at 25 .℃
Buffer in pharmaceutical and biologic sys-tems
36
Buffer in pharmaceutical and biologic sys-tems• Example
At pH 7.4
C11H16N2O2 + H2O C11H16N2O2H+ + OH-
(Pilocarpine base)
(Pilocarpine ion)
pH= pKw- pKb + log
[base] [salt]
At pH 4.0
7.4 = 14 – 7.15 + log [base] [salt]
[base] [salt] = 3.56 / 1
Mole percent of base =
3.56 / (1 + 3.56) • 100 = 78%
4.0 = 14 – 7.15 + log
[base] [salt] = 0.0014 / 1
Mole percent of base =
0.0014 / (1 + 0.0014) • 100 = 0.13%
[base] [salt]
37
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
38
Buffered isotonic solu-tion
Red blood cell
NaCl solution 2.0 %Hypertonic,
Shrink
0.9 %Isotonic
0.2 %Hypotonic,Hemolysis
39
Buffered isotonic solu-tion• The term Isotonic should be restricted to
solutions having equal osmotic pressures which respect to a particular membrane (Husa)
• Isotonicity value…the concentration of an aqueous NaCl soln. having the same col-ligative properties as soln. (Goyan & Reck)
40
Measurement of tonicity• Hemolytic method
…apply red blood cells
…based on the fact that a hypotonic soln. liberates oxyhemoglobin in direct proportion to the number of cells hemolyzed
• determine colligative properties (chapter 5) …modifications of the Hill-Blades Technique
…based on a measurement of the slight temp. differences arising from differences in the vapor pressure of thermally insulated sam-ples contained in constant-humidity chambers
Tf = 0.52 ºC (Freezing point lowering of human blood & lacrimal fluid)
41
Calculating Tonicity Using Liso values
• The Van’t Hoff expression
Tf = L · c
(Chapter 6)
Conc. that is isotonic with body fluids
Liso = Tf / c
0.52 °
Molal freezing point depression
of water
42
Calculating Tonicity Using Liso values
43
Contents
• The Buffer Equation
• Buffer Capacity
• Buffers in
pharmaceutical and Biologic Systems
• Buffered Isotonic Solutions
• Methods of Adjusting Tonicity and pH
44
Method of adjusting tonicity and pHClass I …add Sod. Chloride to lower the
freezing point of soln. to -0.52°
① White-Vincent method
② Sprowls method
① Cryoscopic method ② Sodium chloride equivalent method
Class II …add Water to form an isotonic soln.
45
Class I methods
• Cryoscopic method ( 빙점강하도법 )
(Example)
How much NaCl is required to render 100mL of a 1% soln. of apomorphine HCl isotonic with blood serum?
Δ Tf0.9%
of NaCl soln : 0.52°(Isotonic with blood)
Δ Tf1%
of apomorphine HCl soln : 0.08° (from table)
to reduce the freezing point by an additional 0.44°(0.52-0.08)
Δ Tf1%
of NaCl soln : 0.58°
1(%)/X = 0.58/0.44 ; X = 0.76 (%)
Dissolve 1 g apomorphine HCl + 0.76g NaCl make 100mL soln. with water
46
Class I methods• Sodium chloride equivalent(E)
method ( 염화나트륨당량법 ) by Mellen & Seltzer
1g drug tonicity = Eg NaCl tonicity
ΔTf = Liso · c
ΔTf = Liso · 1g/MWc = 1 g / molec-
ular weight
3.4
58.45
E
E : weight of NaCl with the same freezing point depression as 1g of the drug.
E ≈ 17 · Liso / MW
47
Class II methods
• White-Vincent method
(Example)
GOAL: make 30mL of a 1% soln. of procaine HCl isotonic with body fluid
48
Class II methods
• Steps for White-Vincent method① Weight in grams of drug(0.3 g) • Sod. Chloride
equivalent E(0.21..from table) = quantity of sod. Chloride equivalent to w of drug(0.063 g)
② 0.9 g/100mL = 0.063 g / V③ V = 0.063 • 100/0.9④ V = 7.0 mL⑤ Add isotonic-buffered diluting soln. to complete
V = w • E • 111.1
49
Class II methods
•White vincent method
0.3g drug(E=0.21) 7ml
add 0.9%NaCl
or
Isotonic buffered sol.
30ml
water
0.9%NaCl
isotonic
GOAL: make 30mL of 1% soln.
of procaine HCl iso-tonic with body fluid
50
Class II methods
• Sprowls method
w EV
=0.9 g100 ml
W = 0.3 g (1% solution)
?
TABLE
51
Thank you for your attention