Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
1.
AAPS PharmSciTech ; 18(8): 3227-3235, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28560505

ABSTRACT

Liposomes, the biocompatible lipid bilayer vesicles, have attracted immense attention due to their distinctive features such as efficient vehicle for the delivery of a wide range of therapeutic agents, adjustable formulation properties, and high drug entrapment efficiency. In this contribution, we present a simple method for the preparation of liposomes using glass beads and compared the potential of this method with conventional methods of liposome preparation. The prepared liposomes were characterized by different analytical techniques (HPLC, DLS, TEM, differential scanning calorimetry, and in vitro drug release). Our findings revealed that the particle size of liposomes is mainly dependent on the size of the glass beads and the glass bead shearing time. An average liposome size of 67.7 ± 25.5 nm was obtained using 2-mm glass beads after 24-h incubation at 200 rpm. The liposomes prepared under the optimized conditions exhibited a high encapsulation efficiency of 92.1 ± 1.7% with 31.08% drug release after 360 min at 37°C. In conclusion, the developed method is a simple and convenient process of liposome preparation of different sizes with desirable entrapment efficiency capacity.


Subject(s)
Glass/chemistry , Liposomes/chemical synthesis , Liposomes/economics , Particle Size , Amphotericin B/chemical synthesis , Amphotericin B/economics , Calorimetry, Differential Scanning/economics , Calorimetry, Differential Scanning/methods , Chemistry, Pharmaceutical/economics , Chemistry, Pharmaceutical/methods , Cholesterol/chemical synthesis , Cholesterol/economics , Cost-Benefit Analysis , Phosphatidylcholines/chemical synthesis , Phosphatidylcholines/economics , Shear Strength
2.
J Manag Care Spec Pharm ; 20(8): 851-61, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25062079

ABSTRACT

BACKGROUND: Medication adherence, defined as taking medications as prescribed, is a key component in controlling disease progression and managing chronic illnesses such as diabetes, hypertension, and high blood cholesterol. These diseases constitute 3 of the top 5 most prevalent conditions among Medicare beneficiaries, warranting further attention to find ways to promote better medication adherence. The scientific literature has established the clinical and financial benefits of medication adherence and the role of dispensing channel in impacting adherence to medications. However, a common limitation in channel-adherence studies is the failure to control for healthy adherer effect (HAE), referring to individuals who are likely to engage proactively in activities that improve their adherence. Healthier individuals may choose the home-delivery channel to ensure continuity in their medication regimens and to minimize obstacles to adherence, such as inadequate access, inconvenience, and financial concerns. Thus, better medication adherence in home delivery may reflect healthier patients' predisposition to self-select for home delivery options. To accurately attribute the impact of dispensing channel on adherence, research would need to control for bias from a patient's predisposition to be adherent.  OBJECTIVE: To examine the association of pharmacy dispensing channel (home delivery or retail pharmacy) with medication adherence for Medicare Part D beneficiaries taking medications for diabetes, hypertension, or high blood cholesterol, while controlling for low-income subsidy status, differences in days supply, and prior adherence behavior (PAB) as a way to partly control for HAE. METHODS: A retrospective analysis using de-identified pharmacy claims data from a large national pharmacy benefits manager between October 2010 and December 2012. Continuously eligible Medicare Part D beneficiaries (Medicare Advantage and prescription drug plans participants only) aged 65 years or older who had an antidiabetic, antihypertensive, or antihyperlipidemic prescription claim between October and December 2010, were identified and followed for the next 2 years. Those enrolled in a home delivery auto refill program were excluded from this analysis. Multivariate logistic regression was used to evaluate the impact of dispensing channel on medication adherence, controlling for differences in demographics, low-income subsidy status, disease burden, and drug-use pattern. Patients with a proportion of days covered of ≥ 80% were considered to be adherent. The analysis controlled for PAB by using patients' adherence status in the year 2011.  RESULTS: The final analytical samples consisted of 150,389 diabetic patients, 615,618 hypertension patients, and 358,795 high blood cholesterol patients. The adjusted odds of being adherent for beneficiaries using home delivery were 1.25 times higher (CI = 1.20-1.30) for diabetes medications, 1.29 times higher (CI = 1.27-1.32) for hypertension medications, and 1.26 times higher (CI = 1.23-1.29) for high blood cholesterol medications, compared with beneficiaries using retail channels to obtain their prescriptions. PAB was the strongest contributor to the odds of a patient being adherent across all 3 therapy classes, ranging from odds ratio of 4.48 to 8.09.  CONCLUSIONS: After excluding patients who received any prescriptions via home delivery auto refill programs and controlling for PAB, differences in days supply, low-income subsidy status, demographics, and disease burden, Medicare beneficiaries who use home delivery for antidiabetics, antihypertensives, or antihyperlipidemics have a greater likelihood of being adherent than patients who fill their prescriptions at retail. The results of this study provide evidence that where medications are received may impact adherence, even when controlling for PAB. Use of the home delivery dispensing channel may be an effective method to improve adherence for Medicare beneficiaries.


Subject(s)
Delivery of Health Care/methods , Diabetes Mellitus/drug therapy , Hypercholesterolemia/drug therapy , Hypertension/drug therapy , Medication Adherence , Aged , Antihypertensive Agents/economics , Antihypertensive Agents/therapeutic use , Cholesterol/blood , Cholesterol/economics , Delivery of Health Care/economics , Diabetes Mellitus/economics , Female , Humans , Hypercholesterolemia/economics , Hypertension/economics , Hypoglycemic Agents/economics , Hypoglycemic Agents/therapeutic use , Insurance Benefits/economics , Male , Medicare/economics , Medicare Part D/economics , Pharmaceutical Services/economics , Pharmacies/economics , Retrospective Studies , United States
3.
J Occup Environ Med ; 53(7): 799-805, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21691219

ABSTRACT

OBJECTIVE: To examine the relationship between health risks and absenteeism and drug costs vis-a-vis comprehensive workplace wellness. METHODS: Eleven health risks, and change in drug claims, short-term and general illness calculated across four risk change groups. Wellness score examined using Wilcoxon test and regression model for cost change. RESULTS: The results showed 31% at risk; 9 of 11 risks associated with higher drug costs. Employees moving from low to high risk showed highest relative increase (81%) in drug costs; moving from high to low had lowest (24%). Low-high had highest increase in absenteeism costs (160%). With each risk increase, absenteeism costs increased by $CDN248 per year (P < 0.05) with average decrease of 0.07 risk factors and savings $CDN6979 per year. CONCLUSIONS: Both high-risk reduction and low-risk maintenance are important to contain drug costs. Only low-risk maintenance also avoids absenteeism costs associated with high risks.


Subject(s)
Government Agencies/economics , Health Promotion/economics , Absenteeism , Adult , Blood Pressure/drug effects , Body Mass Index , Canada , Cholesterol/blood , Cholesterol/economics , Drug Costs , Female , Health Status Indicators , Humans , Male , Middle Aged , Pilot Projects , Waist Circumference/drug effects , Workplace/economics
4.
J Drugs Dermatol ; 10(5): 531-7, 2011 May.
Article in English | MEDLINE | ID: mdl-21533301

ABSTRACT

BACKGROUND: Atopic dermatitis (AD) is a prevalent skin disorder with significant cost of treatment. Several prescription device moisturizers have been approved by the FDA to treat AD but are significantly more expensive than well-crafted over-the-counter (OTC) moisturizers. No studies have been performed to compare both the clinical efficacy and cost-efficacy of these prescription devices to OTC moisturizers. PURPOSE: The purpose of this study is to compare the clinical efficacy and cost-efficacy of a glycyrrhetinic acid-containing barrier repair cream (BRC-Gly, Atopiclair®), a ceramide-dominant barrier repair cream (BRC-Cer, EpiCeram®) and an OTC petroleum-based skin protectant moisturizer (OTC-Pet, Aquaphor Healing Ointment®) as monotherapy for mild-to-moderate AD in children. METHODS: Thirty-nine patients, age 2-17 years, with mild-to-moderate AD were randomized 1:1:1 to receive one of three treatments-BRC-Gly, BRC-Cer or OTC-Pet-with instructions to apply the treatment three times daily for three weeks. Disease severity and improvement was assessed at baseline and on days 7 and 21. RESULTS: No statistically significant difference for any efficacy assessment was found between the three groups at each time point. The OTC-Pet was found to be at least 47 times more cost-effective than BRC-Gly or BRC-Cer. LIMITATIONS: The relatively small sample size of 39 subjects was not sufficient to establish OTC-Pet as superior treatment in AD. CONCLUSIONS: OTC-Pet is as effective in treating mild-to-moderate AD as both BRC-Gly and BRC-Cer and is at least 47 times more cost-effective. NAME OF REGISTRY: II-AF-ATD-Aquaphor, Comparing the Efficacy and Cost-Effectiveness of Aquaphor to Atopiclair and EpiCeram in Children with Mild to Moderate Atopic Dermatitis. REGISTRATION IDENTIFIER: NCT01093469.


Subject(s)
Dermatitis, Atopic/drug therapy , Dermatologic Agents/therapeutic use , Emollients/therapeutic use , Administration, Cutaneous , Adolescent , Ceramides/administration & dosage , Ceramides/economics , Ceramides/therapeutic use , Child , Child, Preschool , Cholesterol/administration & dosage , Cholesterol/economics , Cholesterol/therapeutic use , Cost-Benefit Analysis , Dermatitis, Atopic/pathology , Dermatologic Agents/administration & dosage , Dermatologic Agents/economics , Dietary Fats/administration & dosage , Dietary Fats/economics , Dietary Fats/therapeutic use , Double-Blind Method , Drug Combinations , Emollients/administration & dosage , Emollients/economics , Fatty Acids/administration & dosage , Fatty Acids/economics , Fatty Acids/therapeutic use , Female , Glycyrrhetinic Acid/administration & dosage , Glycyrrhetinic Acid/economics , Glycyrrhetinic Acid/therapeutic use , Humans , Male , Nonprescription Drugs/administration & dosage , Nonprescription Drugs/economics , Nonprescription Drugs/therapeutic use , Petrolatum/administration & dosage , Petrolatum/economics , Petrolatum/therapeutic use , Plant Extracts/administration & dosage , Plant Extracts/economics , Plant Extracts/therapeutic use , Prescription Drugs/administration & dosage , Prescription Drugs/economics , Prescription Drugs/therapeutic use , Severity of Illness Index , Treatment Outcome
7.
Pharmacoeconomics ; 5(3): 238-48, 1994 Mar.
Article in English | MEDLINE | ID: mdl-10146898

ABSTRACT

The purpose of this study was to demonstrate a new method of estimating the cost effectiveness of interventions that lower blood cholesterol levels in the prevention of coronary heart disease (CHD) at the community level. The participants in the study were 67 651 men aged 35 to 64 years in the Lower Hunter region of New South Wales, Australia. Census data, risk factor profiles and CHD event rates from community surveillance, plus costs in 1988-1989 Australian dollars, were used as inputs to a computer program that used a logistic equation. The output estimated the CHD events avoided and the cost effectiveness of an intervention that identified and treated men with cholesterol levels greater than 6.5 mmol/L with dietary modification and cholestyramine. The cost of implementation of the intervention was $A50.1 million to prevent 104 CHD events. The cost-effectiveness ratio was $A482 224 per CHD event avoided (SD = $A24 761) and the direct medical costs avoided were approximately $A500 000 over a 5-year period ($A4535.07 per CHD event avoided). Drug acquisition costs contributed substantially (88%) to the total costs of interventions that rely on screening to identify individuals with high cholesterol for intensive treatment.


Subject(s)
Cholesterol , Coronary Disease/prevention & control , Adult , Australia , Cholesterol/blood , Cholesterol/economics , Coronary Disease/economics , Costs and Cost Analysis , Humans , Logistic Models , Male , Middle Aged , Risk Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...